Trial Outcomes & Findings for Epidemiology Study of Malaria Transmission Intensity in Africa (NCT NCT01190202)

NCT ID: NCT01190202

Last Updated: 2020-08-18

Results Overview

The Overall parasite prevalence (PP) data were collected across centers from subjects aged between and including: 6 months to 4 Years (6M-4Y), 5 to 19 Years (5-19 Y) and 20 Years or older (20Y+), for each Survey. The number of subjects P. Falciparum parasitemia infected among the number of subjects with known result for P.falciparum parasitemia test was tabulated.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

21618 participants

Primary outcome timeframe

At each Survey visit

Results posted on

2020-08-18

Participant Flow

For each year and each site, approximately 400 subjects at least 6 months and \< 5 years old, approximately 200 subjects at least 5 years and \< 20 years old and approximately 200 subjects at least 20 years old were to be enrolled. The study was conducted at 8 sites and 6 countries for the first 3 surveys and 3 sites from 3 countries for Survey 4.

Participant milestones

Participant milestones
Measure
Overall Study Group (Survey 1)
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study
STARTED
6404
6414
6400
2400
Overall Study
COMPLETED
6404
6414
6400
2400
Overall Study
NOT COMPLETED
0
0
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Race and Ethnicity were not collected from any participant.

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Overall Study Group (Survey 1)
n=6404 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=6414 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6400 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=2400 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Total
n=21618 Participants
Total of all reporting groups
Age, Continuous
12.6 Years
STANDARD_DEVIATION 14.6 • n=6404 Participants
12.1 Years
STANDARD_DEVIATION 14.3 • n=6414 Participants
12.1 Years
STANDARD_DEVIATION 14.2 • n=6400 Participants
12.4 Years
STANDARD_DEVIATION 14.4 • n=2400 Participants
12.28 Years
STANDARD_DEVIATION 14.37 • n=21618 Participants
Sex: Female, Male
Female
3670 Participants
n=6404 Participants
3791 Participants
n=6414 Participants
3752 Participants
n=6400 Participants
1420 Participants
n=2400 Participants
12633 Participants
n=21618 Participants
Sex: Female, Male
Male
2734 Participants
n=6404 Participants
2623 Participants
n=6414 Participants
2648 Participants
n=6400 Participants
980 Participants
n=2400 Participants
8985 Participants
n=21618 Participants
Race and Ethnicity Not Collected
0 Participants
Race and Ethnicity were not collected from any participant.

PRIMARY outcome

Timeframe: At each Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The Overall parasite prevalence (PP) data were collected across centers from subjects aged between and including: 6 months to 4 Years (6M-4Y), 5 to 19 Years (5-19 Y) and 20 Years or older (20Y+), for each Survey. The number of subjects P. Falciparum parasitemia infected among the number of subjects with known result for P.falciparum parasitemia test was tabulated.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=6401 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=6411 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6400 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=2399 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), for Each Survey
6M-4Y, Overall
720 Participants
574 Participants
605 Participants
345 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), for Each Survey
5-19Y, Overall
446 Participants
469 Participants
483 Participants
278 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), for Each Survey
20+Y, Overall
147 Participants
146 Participants
193 Participants
92 Participants

SECONDARY outcome

Timeframe: At each Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall parasite prevalence (PP) data were collected across centers from subjects aged 4 years or less, for each Survey. The number of subjects P. Falciparum parasitemia infected among the number of subjects with known result for P.falciparum parasitemia test was tabulated.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=3200 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=3197 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=3193 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=1193 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), According to Annual Age for Children of 4 Years or Less, for Each Survey
Children aged 4 years
243 Participants
165 Participants
176 Participants
86 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), According to Annual Age for Children of 4 Years or Less, for Each Survey
Children aged 0 year
21 Participants
38 Participants
41 Participants
25 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), According to Annual Age for Children of 4 Years or Less, for Each Survey
Children aged 1 year
94 Participants
75 Participants
128 Participants
62 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), According to Annual Age for Children of 4 Years or Less, for Each Survey
Children aged 2 years
139 Participants
122 Participants
125 Participants
86 Participants
Number of Subjects With Plasmodium Falciparum (P. Falciparum) Parasitaemia (PFP), According to Annual Age for Children of 4 Years or Less, for Each Survey
Children aged 3 years
223 Participants
174 Participants
135 Participants
86 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall anemia and severe anemia data were collected across centers from subjects, aged between and including: 6M-4Y, 5-19 Y and 20Y+, for each survey. Hemoglobin (Hgb) cut-offs used to define anemia and severe anemia in people living at sea level are: Anemia: children 6M to 5Y, Hgb lower than (\<) 11 gram per deciliter (g/dL); children 5-11Y, Hgb \<11.5 g/dL; children 12-13Y, Hgb \<12 g/dL; non-pregnant females, Hgb \<12 g/dL; pregnant females, Hgb \<11 g/dL; males, Hgb \<13 g/dL. Severe anemia: any age or gender, Hgb \<7 g/dL. Missing/ Not applicable (NA) = if age or pregnancy status was not available. Among each age category, results for both sub-categories "Yes" (subjects with anemia) and "Missing/NA" are presented below, results for the category "No" can be deduced from the number of participants analyzed in the corresponding age category, minus (number of "Yes" + number of "Missing/NA"). Similar presentation is followed for "severe anemia" results.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=6401 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=6411 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6400 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=2399 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Severe anemia, 20Y+
915 Participants
956 Participants
944 Participants
287 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Anaemia, 6M-4Y
1974 Participants
2025 Participants
1974 Participants
871 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Anemia, 6M-4Y
4 Participants
2 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Anemia, 5-19Y
806 Participants
794 Participants
765 Participants
371 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Anemia, 5-19Y
2 Participants
2 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Anemia, 20Y+
673 Participants
631 Participants
651 Participants
313 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Anemia, 20Y+
1 Participants
0 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Severe anaemia, 6M-4Y
85 Participants
70 Participants
84 Participants
34 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Severe anemia, 6M-4Y
1226 Participants
1172 Participants
1219 Participants
322 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Severe anaemia, 5-19Y
10 Participants
12 Participants
19 Participants
5 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Missing/NA Severe anemia, 5-19Y
807 Participants
833 Participants
847 Participants
235 Participants
Number of Subjects With Anemia and Severe Anemia for Each Survey
Overall Yes, Severe anaemia, 20Y+
17 Participants
14 Participants
9 Participants
4 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall anti-malaria therapy data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg). Results include the following categories: Malaria treatment (MT) in past 14 days with sub-categories assessed: Yes, No; Exact days of malaria treatment (EDMT) with sub-categories assessed: Ongoing, 1-3 Days, ≥ 4 Days, Missing/NA; Other medication (OM) in past 14 days with sub-categories assessed: Yes, No; Days of other medication (DOM) with sub-categories assessed: Ongoing, 1-7 Days, ≥ 8 Days, Missing/NA; Malaria hospitalization (MH) in the last 3 months with sub-categories assessed: Yes, No. Missing/NA = Missing or Not Applicable.\* In case of several medication (malaria treatment or other medication) taken per subject, the maximum duration was computed for this study.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, MT in past 14 days, Yes
22 Participants
9 Participants
2 Participants
12 Participants
262 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, MT in past 14 days, No
351 Participants
161 Participants
56 Participants
107 Participants
2218 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, EDMT *, ≥ 4days
1 Participants
2 Participants
0 Participants
3 Participants
27 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, EDMT *, Missing/Not applicable
351 Participants
161 Participants
56 Participants
107 Participants
2219 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, MH in the last 3 months, No
366 Participants
166 Participants
57 Participants
112 Participants
2390 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, OM in past 14 days, No
265 Participants
59 Participants
15 Participants
51 Participants
1024 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, DOM *, Ongoing
4 Participants
1 Participants
1 Participants
2 Participants
17 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, DOM *, 1-7 days
25 Participants
11 Participants
7 Participants
5 Participants
125 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, OM in past 14 days, No
99 Participants
11 Participants
9 Participants
1238 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, DOM *, Ongoing
5 Participants
1 Participants
1 Participants
41 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, DOM *, 1-7 days
15 Participants
5 Participants
1 Participants
158 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, DOM *, Missing/Not applicable
99 Participants
11 Participants
9 Participants
1240 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, EDMT *, Ongoing
3 Participants
2 Participants
0 Participants
0 Participants
28 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, EDMT *, 1-3 days
18 Participants
5 Participants
2 Participants
9 Participants
206 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, OM in past 14 days, Yes
35 Participants
33 Participants
21 Participants
33 Participants
445 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, OM in past 14 days, No
338 Participants
137 Participants
37 Participants
86 Participants
2035 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, DOM *, Ongoing
8 Participants
7 Participants
2 Participants
5 Participants
79 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, DOM *, 1-7 days
25 Participants
26 Participants
19 Participants
27 Participants
365 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, DOM *, Missing/Not applicable
340 Participants
137 Participants
37 Participants
87 Participants
2035 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
6M-4Y, MH in the last 3 months, Yes
7 Participants
4 Participants
1 Participants
7 Participants
90 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, MT in past 14 days, Yes
5 Participants
6 Participants
4 Participants
2 Participants
85 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, MT in past 14 days, No
289 Participants
65 Participants
19 Participants
56 Participants
1082 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, EDMT *, Ongoing
1 Participants
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, EDMT *, 1-3 days
4 Participants
6 Participants
4 Participants
1 Participants
75 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
1 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, EDMT *, Missing/Not applicable
289 Participants
65 Participants
19 Participants
56 Participants
1082 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, OM in past 14 days, Yes
29 Participants
12 Participants
8 Participants
7 Participants
143 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, DOM *, Missing/Not applicable
265 Participants
59 Participants
15 Participants
51 Participants
1025 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, MH in the last 3 months, Yes
0 Participants
3 Participants
0 Participants
1 Participants
24 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
5-19Y, MH in the last 3 months, No
294 Participants
68 Participants
23 Participants
57 Participants
1143 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, MT in past 14 days, Yes
1 Participants
0 Participants
0 Participants
102 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, MT in past 14 days, No
118 Participants
17 Participants
11 Participants
1339 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, EDMT *, Ongoing
0 Participants
0 Participants
0 Participants
14 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, EDMT *, 1-3 days
1 Participants
0 Participants
0 Participants
80 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, EDMT *, Missing/Not applicable
118 Participants
17 Participants
11 Participants
1339 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, OM in past 14 days, Yes
20 Participants
6 Participants
2 Participants
203 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, MH in the last 3 months, Yes
0 Participants
2 Participants
0 Participants
18 Participants
Number of Subjects With Anti-malarial Therapy in Survey 1, According to Parasite Density
20Y+, MH in the last 3 months, No
119 Participants
15 Participants
11 Participants
1423 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall anti-malaria therapy data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg). Results include the following categories: Malaria treatment (MT) in past 14 days with sub-categories assessed: Yes, No; Exact days of malaria treatment (EDMT) with sub-categories assessed: Ongoing, 1-3 Days, ≥ 4 Days, Missing/NA; Other medication (OM) in past 14 days with sub-categories assessed: Yes, No; Days of other medication (DOM) with sub-categories assessed: Ongoing, 1-7 Days, ≥ 8 Days, Missing/NA; Malaria hospitalization (MH) in the last 3 months with sub-categories assessed: Yes, No. Missing/NA = Missing or Not Applicable.\* In case of several medication (malaria treatment or other medication) taken per subject, the maximum duration was computed for this study.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, EDMT *, 1-3 days
12 Participants
1 Participants
1 Participants
4 Participants
206 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, DOM *, 1-7 days
30 Participants
9 Participants
6 Participants
15 Participants
410 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, DOM *, Missing/NA
241 Participants
133 Participants
58 Participants
59 Participants
2088 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, MH in the last 3 months, Yes
3 Participants
3 Participants
2 Participants
3 Participants
77 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, MH in the last 3 months, No
280 Participants
145 Participants
65 Participants
73 Participants
2546 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, MT in past 14 days, Yes
11 Participants
3 Participants
2 Participants
4 Participants
77 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, MT in past 14 days, No
322 Participants
68 Participants
27 Participants
32 Participants
1081 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, EDMT *, Ongoing
1 Participants
1 Participants
0 Participants
0 Participants
11 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, EDMT *, 1-3 days
8 Participants
1 Participants
2 Participants
4 Participants
66 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, EDMT *, ≥ 4days
2 Participants
1 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, EDMT *, Missing/NA
322 Participants
68 Participants
27 Participants
32 Participants
1081 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, OM in past 14 days, Yes
33 Participants
10 Participants
8 Participants
9 Participants
134 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, OM in past 14 days, No
300 Participants
61 Participants
21 Participants
27 Participants
1024 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, DOM *, Ongoing
7 Participants
1 Participants
0 Participants
1 Participants
30 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, DOM *, 1-7 days
26 Participants
9 Participants
8 Participants
8 Participants
102 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, DOM *, Missing/NA
300 Participants
61 Participants
21 Participants
27 Participants
1024 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, MH in the last 3 months, Yes
5 Participants
1 Participants
1 Participants
1 Participants
19 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
5-19Y, MH in the last 3 months, No
328 Participants
70 Participants
28 Participants
35 Participants
1139 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, MT in past 14 days, Yes
2 Participants
0 Participants
0 Participants
2 Participants
84 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, MT in past 14 days, No
122 Participants
10 Participants
5 Participants
5 Participants
1357 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, EDMT *, Ongoing
0 Participants
0 Participants
0 Participants
1 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, EDMT *, 1-3 days
2 Participants
0 Participants
0 Participants
1 Participants
72 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, EDMT *, Missing/NA
122 Participants
10 Participants
5 Participants
5 Participants
1357 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, OM in past 14 days, Yes
10 Participants
2 Participants
2 Participants
3 Participants
214 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, OM in past 14 days, No
114 Participants
8 Participants
3 Participants
4 Participants
1227 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, DOM *, Ongoing
1 Participants
0 Participants
1 Participants
2 Participants
71 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, DOM *, 1-7 days
9 Participants
2 Participants
1 Participants
1 Participants
138 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, DOM *, Missing/NA
114 Participants
8 Participants
3 Participants
4 Participants
1227 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, MH in the last 3 months, Yes
1 Participants
1 Participants
0 Participants
0 Participants
19 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
20Y+, MH in the last 3 months, No
123 Participants
9 Participants
5 Participants
7 Participants
1422 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, MT in past 14 days, Yes
14 Participants
6 Participants
2 Participants
5 Participants
257 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, MT in past 14 days, No
269 Participants
142 Participants
65 Participants
71 Participants
2366 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, EDMT *, Ongoing
1 Participants
3 Participants
0 Participants
1 Participants
25 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, EDMT *, ≥ 4days
1 Participants
2 Participants
1 Participants
0 Participants
26 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, EDMT *, Missing/NA
269 Participants
142 Participants
65 Participants
71 Participants
2366 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, OM in past 14 days, Yes
42 Participants
15 Participants
9 Participants
17 Participants
535 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, OM in past 14 days, No
241 Participants
133 Participants
58 Participants
59 Participants
2088 Participants
Number of Subjects With Anti-malarial Therapy in Survey 2, According to Parasite Density
6M-4Y, DOM *, Ongoing
12 Participants
6 Participants
3 Participants
2 Participants
118 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall anti-malaria therapy data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg). Results include the following categories: Malaria treatment (MT) in past 14 days with sub-categories assessed: Yes, No; Exact days of malaria treatment (EDMT) with sub-categories assessed: Ongoing, 1-3 Days, ≥ 4 Days, Missing/NA; Other medication (OM) in past 14 days with sub-categories assessed: Yes, No; Days of other medication (DOM) with sub-categories assessed: Ongoing, 1-7 Days, ≥ 8 Days, Missing/NA; Malaria hospitalization (MH) in the last 3 months with sub-categories assessed: Yes, No. Missing/NA = Missing or Not Applicable.\* In case of several medication (malaria treatment or other medication) taken per subject, the maximum duration was computed for this study.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, MT in past 14 days, No
262 Participants
148 Participants
71 Participants
82 Participants
2321 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, MT in past 14 days, Yes
14 Participants
4 Participants
1 Participants
1 Participants
58 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, DOM *, Missing/NA
297 Participants
76 Participants
10 Participants
22 Participants
1001 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, MH in the last 3 months, Yes
7 Participants
0 Participants
0 Participants
1 Participants
17 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, MH in the last 3 months, No
334 Participants
94 Participants
13 Participants
34 Participants
1112 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, EDMT *, 1-3 days
5 Participants
1 Participants
0 Participants
0 Participants
63 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, EDMT *, Missing/NA
166 Participants
11 Participants
5 Participants
4 Participants
1332 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, MT in past 14 days, Yes
17 Participants
13 Participants
3 Participants
9 Participants
267 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, EDMT *, Ongoing
4 Participants
1 Participants
0 Participants
4 Participants
33 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, EDMT *, 1-3 days
11 Participants
10 Participants
3 Participants
5 Participants
210 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, EDMT *, ≥ 4days
2 Participants
2 Participants
0 Participants
0 Participants
24 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, EDMT *, Missing/NA
262 Participants
148 Participants
71 Participants
82 Participants
2321 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, OM in past 14 days, Yes
65 Participants
30 Participants
18 Participants
18 Participants
547 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, OM in past 14 days, No
214 Participants
131 Participants
56 Participants
73 Participants
2041 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, DOM *, Ongoing
10 Participants
8 Participants
3 Participants
6 Participants
142 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, DOM *, 1-7 days
55 Participants
22 Participants
15 Participants
12 Participants
394 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
11 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, DOM *, Missing/NA
214 Participants
131 Participants
56 Participants
73 Participants
2041 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, MH in the last 3 months, Yes
14 Participants
4 Participants
3 Participants
0 Participants
99 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, MT in past 14 days, No
327 Participants
90 Participants
12 Participants
34 Participants
1071 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
6M-4Y, MH in the last 3 months, No
265 Participants
157 Participants
71 Participants
91 Participants
2489 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, EDMT *, Ongoing
4 Participants
1 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, EDMT *, 1-3 days
8 Participants
3 Participants
1 Participants
1 Participants
50 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, EDMT *, ≥ 4days
2 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, EDMT *, Missing/NA
327 Participants
90 Participants
12 Participants
34 Participants
1071 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, OM in past 14 days, Yes
44 Participants
18 Participants
3 Participants
13 Participants
128 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, OM in past 14 days, No
297 Participants
76 Participants
10 Participants
22 Participants
1001 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, DOM *, Ongoing
13 Participants
1 Participants
0 Participants
2 Participants
19 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, DOM *, 1-7 days
31 Participants
17 Participants
3 Participants
11 Participants
109 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
5-19Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, MT in past 14 days, Yes
5 Participants
2 Participants
0 Participants
0 Participants
70 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, MT in past 14 days, No
166 Participants
11 Participants
5 Participants
4 Participants
1332 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, EDMT *, Ongoing
0 Participants
0 Participants
0 Participants
0 Participants
6 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, EDMT *, ≥ 4days
0 Participants
1 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, OM in past 14 days, Yes
25 Participants
3 Participants
3 Participants
1 Participants
227 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, OM in past 14 days, No
146 Participants
10 Participants
2 Participants
3 Participants
1175 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, DOM *, Ongoing
5 Participants
3 Participants
0 Participants
1 Participants
70 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, DOM *, 1-7 days
19 Participants
0 Participants
3 Participants
0 Participants
151 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, DOM *, ≥ 8 days
1 Participants
0 Participants
0 Participants
0 Participants
6 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, DOM *, Missing/NA
146 Participants
10 Participants
2 Participants
3 Participants
1175 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, MH in the last 3 months, Yes
0 Participants
0 Participants
0 Participants
0 Participants
12 Participants
Number of Subjects With Anti-malarial Therapy in Survey 3, According to Parasite Density
20Y+, MH in the last 3 months, No
171 Participants
13 Participants
5 Participants
4 Participants
1390 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The overall anti-malaria therapy data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg). Results include the following categories: Malaria treatment (MT) in past 14 days with sub-categories assessed: Yes, No; Exact days of malaria treatment (EDMT) with sub-categories assessed: Ongoing, 1-3 Days, ≥ 4 Days, Missing/NA; Other medication (OM) in past 14 days with sub-categories assessed: Yes, No; Days of other medication (DOM) with sub-categories assessed: Ongoing, 1-7 Days, ≥ 8 Days, Missing/NA; Malaria hospitalization (MH) in the last 3 months with sub-categories assessed: Yes, No. Missing/NA = Missing or Not Applicable.\* In case of several medication (malaria treatment or other medication) taken per subject, the maximum duration was computed for this study.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, DOM *, Ongoing
1 Participants
0 Participants
0 Participants
18 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, DOM *, Missing/NA
147 Participants
92 Participants
13 Participants
42 Participants
696 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, MH in the last 3 months, No
159 Participants
102 Participants
20 Participants
52 Participants
820 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, EDMT *, Ongoing
0 Participants
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, MH in the last 3 months, Yes
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, MH in the last 3 months, No
87 Participants
4 Participants
1 Participants
503 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, DOM *, Ongoing
5 Participants
2 Participants
3 Participants
5 Participants
48 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, EDMT *, 1-3 days
3 Participants
1 Participants
1 Participants
1 Participants
49 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, EDMT *, Missing/NA
163 Participants
101 Participants
19 Participants
49 Participants
777 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, OM in past 14 days, Yes
21 Participants
11 Participants
7 Participants
12 Participants
152 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, OM in past 14 days, No
147 Participants
92 Participants
13 Participants
42 Participants
696 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, DOM *, 1-7 days
16 Participants
8 Participants
4 Participants
7 Participants
103 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, DOM *, ≥ 8 days
0 Participants
1 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, MH in the last 3 months, Yes
9 Participants
1 Participants
0 Participants
2 Participants
28 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, MT in past 14 days, Yes
2 Participants
0 Participants
0 Participants
0 Participants
10 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, MT in past 14 days, No
196 Participants
51 Participants
16 Participants
13 Participants
318 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, EDMT *, 1-3 days
2 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, EDMT *, Missing/NA
196 Participants
51 Participants
16 Participants
13 Participants
318 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, OM in past 14 days, Yes
13 Participants
4 Participants
0 Participants
2 Participants
28 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, OM in past 14 days, No
185 Participants
47 Participants
16 Participants
11 Participants
300 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, DOM *, Ongoing
1 Participants
0 Participants
0 Participants
1 Participants
6 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, DOM *, 1-7 days
12 Participants
4 Participants
0 Participants
1 Participants
22 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, DOM *, ≥ 8 days
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, DOM *, Missing/NA
185 Participants
47 Participants
16 Participants
11 Participants
300 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, MH in the last 3 months, Yes
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
5-19Y, MH in the last 3 months, No
198 Participants
51 Participants
16 Participants
13 Participants
326 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, MT in past 14 days, Yes
1 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, MT in past 14 days, No
86 Participants
4 Participants
1 Participants
500 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, EDMT *, Ongoing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, EDMT *, 1-3 days
1 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, EDMT *, ≥ 4days
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, EDMT *, Missing/NA
86 Participants
4 Participants
1 Participants
500 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, OM in past 14 days, Yes
5 Participants
0 Participants
0 Participants
57 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, OM in past 14 days, No
82 Participants
4 Participants
1 Participants
451 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, DOM *, 1-7 days
4 Participants
0 Participants
0 Participants
36 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
20Y+, DOM *, Missing/NA
82 Participants
4 Participants
1 Participants
451 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, MT in past 14 days, Yes
5 Participants
2 Participants
1 Participants
5 Participants
71 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, MT in past 14 days, No
163 Participants
101 Participants
19 Participants
49 Participants
777 Participants
Number of Subjects With Anti-malarial Therapy in Survey 4, According to Parasite Density
6M-4Y, EDMT *, Ongoing
2 Participants
1 Participants
0 Participants
4 Participants
21 Participants

SECONDARY outcome

Timeframe: During the 14 day-period before the malaria treatment

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and who have data available during the past 14 days period of Malaria treatment.

The mean and standard deviation of the number of days of malaria treatment (DMT) were calculated for the past 14 days period of treatment. The malaria treatment data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=24 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=13 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=14 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=401 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Malaria Treatment at Survey 1
6M-4Y, DMT
2.6 Days
Standard Deviation 1.02
3.7 Days
Standard Deviation 1.70
2.5 Days
Standard Deviation 0.71
3.1 Days
Standard Deviation 0.67
3.1 Days
Standard Deviation 1.45
Mean Number of Days With Malaria Treatment at Survey 1
5-19Y, DMT
2.0 Days
Standard Deviation 0.82
2.2 Days
Standard Deviation 0.98
2.8 Days
Standard Deviation 0.50
3.5 Days
Standard Deviation 0.71
2.5 Days
Standard Deviation 1.09
Mean Number of Days With Malaria Treatment at Survey 1
20+Y, DMT
1.0 Days
Standard Deviation 0.00
2.6 Days
Standard Deviation 1.37

SECONDARY outcome

Timeframe: During the 14 day-period before the malaria treatment

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and who have data available during the past 14 days period of Malaria treatment.

The mean and standard deviation of the number of days of malaria treatment (DMT) were calculated for the past 14 days period of treatment. The malaria treatment data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=25 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=5 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=4 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=9 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=377 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Malaria Treatment at Survey 2
6M-4Y, DMT
2.8 Days
Standard Deviation 1.48
5.7 Days
Standard Deviation 2.31
3.5 Days
Standard Deviation 0.71
2.0 Days
Standard Deviation 1.15
3.1 Days
Standard Deviation 1.16
Mean Number of Days With Malaria Treatment at Survey 2
5-19Y, DMT
2.8 Days
Standard Deviation 1.81
3.5 Days
Standard Deviation 2.12
3.0 Days
Standard Deviation 0.00
2.5 Days
Standard Deviation 1.00
2.5 Days
Standard Deviation 0.81
Mean Number of Days With Malaria Treatment at Survey 2
20+Y, DMT
3.0 Days
Standard Deviation 0.00
1.0 Days
Standard Deviation 0.00
2.5 Days
Standard Deviation 1.37

SECONDARY outcome

Timeframe: During the 14 day-period before the malaria treatment

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and who have data available during the past 14 days period of Malaria treatment.

The mean and standard deviation of the number of days of malaria treatment (DMT) were calculated for the past 14 days period of treatment. The malaria treatment data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=28 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=17 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=4 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=6 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=352 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Malaria Treatment at Survey 3
6M-4Y, DMT
3.0 Days
Standard Deviation 0.71
3.3 Days
Standard Deviation 1.07
2.3 Days
Standard Deviation 1.15
2.2 Days
Standard Deviation 1.10
3.1 Days
Standard Deviation 1.08
Mean Number of Days With Malaria Treatment at Survey 3
5-19Y, DMT
3.9 Days
Standard Deviation 2.88
1.7 Days
Standard Deviation 1.15
3.0 Days
Standard Deviation 0.00
1.0 Days
Standard Deviation 0.00
2.9 Days
Standard Deviation 1.27
Mean Number of Days With Malaria Treatment at Survey 3
20+Y, DMT
1.4 Days
Standard Deviation 0.89
5.0 Days
Standard Deviation 2.83
2.3 Days
Standard Deviation 1.12

SECONDARY outcome

Timeframe: During the 14 day-period before the malaria treatment

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and who have data available during the past 14 days period of Malaria treatment.

The mean and standard deviation of the number of days of malaria treatment (DMT) were calculated for the past 14 days period of treatment. The malaria treatment data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=6 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=1 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=1 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=1 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=64 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Malaria Treatment at Survey 4
6M-4Y, DMT
2.3 Days
Standard Deviation 1.15
3.0 Days
Standard Deviation 0.00
3.0 Days
Standard Deviation 0.00
1.0 Days
Standard Deviation 0.00
3.1 Days
Standard Deviation 0.59
Mean Number of Days With Malaria Treatment at Survey 4
5-19Y, DMT
3.0 Days
Standard Deviation 0.00
2.9 Days
Standard Deviation 0.38
Mean Number of Days With Malaria Treatment at Survey 4
20+Y, DMT
1.0 Days
Standard Deviation 0.00
3.3 Days
Standard Deviation 2.14

SECONDARY outcome

Timeframe: In the last 24 hours or at the survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Measured characteristics of fever were the following: Fever in the last 24 hours (F 24h) and Fever at visit (F at V). Note: Fever set to "Yes" if temperature recorded after axillary conversion was ≥ 37.5 degrees Celsius (°C). Missing/NA = Missing or Not Applicable. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
6M-4Y, F at V - Missing/NA
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
20+Y, F 24h - No
89 Participants
8 Participants
9 Participants
1260 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
20+Y, F at V - Yes
3 Participants
0 Participants
1 Participants
23 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
6M-4Y, F 24h - Yes
71 Participants
53 Participants
21 Participants
60 Participants
361 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
6M-4Y, F 24h - No
302 Participants
117 Participants
37 Participants
59 Participants
2119 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
6M-4Y, F at V - Yes
26 Participants
13 Participants
7 Participants
22 Participants
79 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
6M-4Y, F at V - No
347 Participants
157 Participants
51 Participants
97 Participants
2400 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
5-19Y, F 24h - Yes
37 Participants
25 Participants
10 Participants
24 Participants
124 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
5-19Y, F 24h - No
257 Participants
46 Participants
13 Participants
34 Participants
1043 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
5-19Y, F at V - Yes
6 Participants
5 Participants
5 Participants
17 Participants
29 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
5-19Y, F at V - No
288 Participants
66 Participants
18 Participants
41 Participants
1138 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
20+Y, F 24h - Yes
30 Participants
9 Participants
2 Participants
181 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
20+Y, F at V - No
115 Participants
17 Participants
10 Participants
1418 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 1
20+Y, F at V - Missing/NA
1 Participants
0 Participants
0 Participants
0 Participants

SECONDARY outcome

Timeframe: In the last 24 hours or at the survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Measured characteristics of fever were the following: Fever in the last 24 hours (F 24h) and Fever at visit (F at V). Note: Fever set to "Yes" if temperature recorded after axillary conversion was ≥ 37.5 degrees Celsius (°C). Missing/NA = Missing or Not Applicable. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
6M-4Y, F at V - No
257 Participants
132 Participants
52 Participants
47 Participants
2525 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
20+Y, F at V - No
114 Participants
10 Participants
5 Participants
6 Participants
1404 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
20+Y, F at V - Missing/NA
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
6M-4Y, F 24h - Yes
41 Participants
23 Participants
15 Participants
35 Participants
357 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
6M-4Y, F 24h - No
242 Participants
125 Participants
52 Participants
41 Participants
2266 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
6M-4Y, F at V - Yes
26 Participants
16 Participants
15 Participants
29 Participants
98 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
5-19Y, F 24h - Yes
39 Participants
11 Participants
11 Participants
13 Participants
115 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
5-19Y, F 24h - No
294 Participants
60 Participants
18 Participants
23 Participants
1043 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
5-19Y, F at V - Yes
24 Participants
4 Participants
3 Participants
8 Participants
26 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
5-19Y, F at V - No
309 Participants
67 Participants
26 Participants
28 Participants
1132 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
20+Y, F 24h - Yes
14 Participants
4 Participants
3 Participants
2 Participants
169 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
20+Y, F 24h - No
110 Participants
6 Participants
2 Participants
5 Participants
1272 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 2
20+Y, F at V - Yes
10 Participants
0 Participants
0 Participants
1 Participants
36 Participants

SECONDARY outcome

Timeframe: In the last 24 hours or at the survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Measured characteristics of fever were the following: Fever in the last 24 hours (F 24h) and Fever at visit (F at V). Note: Fever set to "Yes" if temperature recorded after axillary conversion was ≥ 37.5 degrees Celsius (°C). Missing/NA = Missing or Not Applicable. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
6M-4Y, F 24h - Yes
60 Participants
44 Participants
28 Participants
44 Participants
360 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
6M-4Y, F at V - Yes
8 Participants
16 Participants
9 Participants
22 Participants
56 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
6M-4Y, F at V - No
271 Participants
145 Participants
65 Participants
69 Participants
2532 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
5-19Y, F at V - No
330 Participants
87 Participants
12 Participants
21 Participants
1107 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
5-19Y, F at V - Missing/NA
0 Participants
1 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
20+Y, F 24h - Yes
20 Participants
4 Participants
4 Participants
1 Participants
167 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
20+Y, F at V - No
166 Participants
13 Participants
2 Participants
3 Participants
1378 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
20+Y, F at V - Missing/NA
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
6M-4Y, F 24h - No
219 Participants
117 Participants
46 Participants
47 Participants
2228 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
5-19Y, F 24h - Yes
54 Participants
25 Participants
4 Participants
17 Participants
92 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
5-19Y, F 24h - No
287 Participants
69 Participants
9 Participants
18 Participants
1037 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
5-19Y, F at V - Yes
11 Participants
6 Participants
1 Participants
14 Participants
21 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
20+Y, F 24h - No
151 Participants
9 Participants
1 Participants
3 Participants
1235 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 3
20+Y, F at V - Yes
5 Participants
0 Participants
3 Participants
1 Participants
23 Participants

SECONDARY outcome

Timeframe: In the last 24 hours or at the survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Measured characteristics of fever were the following: Fever in the last 24 hours (F 24h) and Fever at visit (F at V). Note: Fever set to "Yes" if temperature recorded after axillary conversion was ≥ 37.5 degrees Celsius (°C). Missing/NA = Missing or Not Applicable. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
6M-4Y, F 24h - Yes
39 Participants
18 Participants
5 Participants
27 Participants
115 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
5-19Y, F 24h - Yes
38 Participants
8 Participants
4 Participants
4 Participants
22 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
20+Y, F 24h - Yes
11 Participants
0 Participants
0 Participants
25 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
20+Y, F at V - Yes
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
6M-4Y, F 24h - No
129 Participants
85 Participants
15 Participants
27 Participants
733 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
6M-4Y, F at V - Yes
8 Participants
8 Participants
4 Participants
18 Participants
20 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
6M-4Y, F at V - No
160 Participants
95 Participants
16 Participants
36 Participants
827 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
6M-4Y, F at V - Missing/NA
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
5-19Y, F 24h - No
160 Participants
43 Participants
12 Participants
9 Participants
306 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
5-19Y, F at V - Yes
5 Participants
0 Participants
2 Participants
1 Participants
4 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
5-19Y, F at V - No
193 Participants
51 Participants
14 Participants
12 Participants
324 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
20+Y, F 24h - No
76 Participants
4 Participants
1 Participants
483 Participants
Number of Subjects With Fever in the Last 24 Hours or at Visit During Survey 4
20+Y, F at V - No
87 Participants
4 Participants
1 Participants
505 Participants

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and with fever reported in the last 24 hours.

The mean and standard deviation of the number of days ago with fever start (DaFs) were calculated for subjects having fever in the last 24 hours. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=138 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=87 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=31 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=86 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=663 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Fever at Survey 1
6M-4Y, DaFs
2.5 Days
Standard Deviation 2.18
2.6 Days
Standard Deviation 2.23
2.1 Days
Standard Deviation 1.42
2.5 Days
Standard Deviation 4.13
2.3 Days
Standard Deviation 1.77
Mean Number of Days With Fever at Survey 1
5-19Y, DaFs
2.2 Days
Standard Deviation 1.41
2.2 Days
Standard Deviation 1.29
2.7 Days
Standard Deviation 2.06
1.7 Days
Standard Deviation 1.05
2.3 Days
Standard Deviation 1.93
Mean Number of Days With Fever at Survey 1
20+Y, DaFs
2.3 Days
Standard Deviation 1.56
2.3 Days
Standard Deviation 1.87
2.5 Days
Standard Deviation 0.71
2.9 Days
Standard Deviation 3.36

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and with fever reported in the last 24 hours.

The mean and standard deviation of the number of days ago with fever start (DaFs) were calculated for subjects having fever in the last 24 hours. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=94 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=38 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=29 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=50 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=641 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Fever at Survey 2
6M-4Y, DaFs
2.1 Days
Standard Deviation 1.35
2.7 Days
Standard Deviation 1.99
1.4 Days
Standard Deviation 0.51
2.0 Days
Standard Deviation 1.46
2.4 Days
Standard Deviation 1.76
Mean Number of Days With Fever at Survey 2
5-19Y, DaFs
2.5 Days
Standard Deviation 1.62
2.6 Days
Standard Deviation 2.38
2.5 Days
Standard Deviation 2.34
2.1 Days
Standard Deviation 1.80
2.1 Days
Standard Deviation 1.38
Mean Number of Days With Fever at Survey 2
20+Y, DaFs
4.0 Days
Standard Deviation 3.64
2.0 Days
Standard Deviation 1.15
2.0 Days
Standard Deviation 1.00
4.0 Days
Standard Deviation 2.83
3.2 Days
Standard Deviation 2.96

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and with fever reported in the last 24 hours.

The mean and standard deviation of the number of days ago with fever start (DaFs) were calculated for subjects having fever in the last 24 hours. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=134 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=72 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=62 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=619 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Fever at Survey 3
6M-4Y, DaFs
2.3 Days
Standard Deviation 1.90
2.4 Days
Standard Deviation 1.95
2.2 Days
Standard Deviation 1.33
2.1 Days
Standard Deviation 1.37
2.5 Days
Standard Deviation 1.80
Mean Number of Days With Fever at Survey 3
5-19Y, DaFs
2.3 Days
Standard Deviation 1.58
2.8 Days
Standard Deviation 1.63
2.5 Days
Standard Deviation 1.73
1.8 Days
Standard Deviation 0.53
2.7 Days
Standard Deviation 2.21
Mean Number of Days With Fever at Survey 3
20+Y, DaFs
3.0 Days
Standard Deviation 1.81
2.8 Days
Standard Deviation 0.50
3.8 Days
Standard Deviation 2.22
3.0 Days
Standard Deviation 0.00
3.3 Days
Standard Deviation 4.28

SECONDARY outcome

Timeframe: During the survey period (approximatively 1 year)

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit and with fever reported in the last 24 hours.

The mean and standard deviation of the number of days ago with fever start (DaFs) were calculated for subjects having fever in the last 24 hours. Fever data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=88 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=26 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=9 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=31 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=162 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Days With Fever at Survey 4
6M-4Y, DaFs
2.2 Days
Standard Deviation 1.05
2.4 Days
Standard Deviation 2.43
1.6 Days
Standard Deviation 0.89
2.2 Days
Standard Deviation 1.64
2.7 Days
Standard Deviation 1.88
Mean Number of Days With Fever at Survey 4
5-19Y, DaFs
2.0 Days
Standard Deviation 0.97
3.8 Days
Standard Deviation 2.38
1.5 Days
Standard Deviation 0.58
2.0 Days
Standard Deviation 1.15
2.1 Days
Standard Deviation 1.23
Mean Number of Days With Fever at Survey 4
20+Y, DaFs
2.5 Days
Standard Deviation 1.21
3.2 Days
Standard Deviation 1.38

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The mean and standard deviation of the axillary temperature at visit (A temp. at V) were calculated. Axillary temperature data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=785 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5087 Participants
Subjects from Survey 1 not infected with P.falciparum.
Axillary Temperature at Visit in Survey 1
20+Y, A temp. at V
36.55 Degrees Celsius
Standard Deviation 0.459
36.70 Degrees Celsius
Standard Deviation 0.387
36.82 Degrees Celsius
Standard Deviation 0.462
36.60 Degrees Celsius
Standard Deviation 0.478
Axillary Temperature at Visit in Survey 1
6M-4Y, A temp. at V
36.65 Degrees Celsius
Standard Deviation 0.521
36.64 Degrees Celsius
Standard Deviation 0.623
36.72 Degrees Celsius
Standard Deviation 0.782
37.04 Degrees Celsius
Standard Deviation 0.803
36.55 Degrees Celsius
Standard Deviation 0.522
Axillary Temperature at Visit in Survey 1
5-19Y, A temp. at V
36.56 Degrees Celsius
Standard Deviation 0.469
36.70 Degrees Celsius
Standard Deviation 0.597
37.07 Degrees Celsius
Standard Deviation 0.853
37.29 Degrees Celsius
Standard Deviation 0.928
36.63 Degrees Celsius
Standard Deviation 0.496

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The mean and standard deviation of axillary temperature at visit (A temp. at V) were calculated. Axillary temperature data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5221 Participants
Subjects from Survey 1 not infected with P.falciparum.
Axillary Temperature at Visit in Survey 2
20+Y, A temp. at V
36.70 Degrees Celsius
Standard Deviation 0.478
36.75 Degrees Celsius
Standard Deviation 0.375
36.64 Degrees Celsius
Standard Deviation 0.559
37.09 Degrees Celsius
Standard Deviation 0.713
36.67 Degrees Celsius
Standard Deviation 0.430
Axillary Temperature at Visit in Survey 2
6M-4Y, A temp. at V
36.69 Degrees Celsius
Standard Deviation 0.574
36.75 Degrees Celsius
Standard Deviation 0.628
36.86 Degrees Celsius
Standard Deviation 0.725
37.41 Degrees Celsius
Standard Deviation 1.201
36.60 Degrees Celsius
Standard Deviation 0.479
Axillary Temperature at Visit in Survey 2
5-19Y, A temp. at V
36.70 Degrees Celsius
Standard Deviation 0.522
36.76 Degrees Celsius
Standard Deviation 0.507
36.76 Degrees Celsius
Standard Deviation 0.773
37.36 Degrees Celsius
Standard Deviation 0.949
36.66 Degrees Celsius
Standard Deviation 0.447

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The mean and standard deviation of axillary temperature at visit (A temp. at V) were calculated. Axillary temperature data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=267 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5117 Participants
Subjects from Survey 1 not infected with P.falciparum.
Axillary Temperature at Visit in Survey 3
6M-4Y, A temp. at V
36.47 Degrees Celsius
Standard Deviation 0.517
36.66 Degrees Celsius
Standard Deviation 0.652
36.68 Degrees Celsius
Standard Deviation 0.701
36.97 Degrees Celsius
Standard Deviation 0.951
36.54 Degrees Celsius
Standard Deviation 0.496
Axillary Temperature at Visit in Survey 3
20+Y, A temp. at V
36.44 Degrees Celsius
Standard Deviation 0.515
36.42 Degrees Celsius
Standard Deviation 0.409
37.54 Degrees Celsius
Standard Deviation 1.135
37.18 Degrees Celsius
Standard Deviation 0.727
36.55 Degrees Celsius
Standard Deviation 0.493
Axillary Temperature at Visit in Survey 3
5-19Y, A temp. at V
36.56 Degrees Celsius
Standard Deviation 0.551
36.66 Degrees Celsius
Standard Deviation 0.571
36.61 Degrees Celsius
Standard Deviation 0.475
37.45 Degrees Celsius
Standard Deviation 1.117
36.59 Degrees Celsius
Standard Deviation 0.462

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The mean and standard deviation of axillary temperature at visit (A temp. at V) were calculated. Axillary temperature data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1683 Participants
Subjects from Survey 1 not infected with P.falciparum.
Axillary Temperature at Visit in Survey 4
6M-4Y, A temp. at V
36.51 Degrees Celsius
Standard Deviation 0.508
36.51 Degrees Celsius
Standard Deviation 0.535
36.95 Degrees Celsius
Standard Deviation 0.927
37.16 Degrees Celsius
Standard Deviation 1.187
36.40 Degrees Celsius
Standard Deviation 0.492
Axillary Temperature at Visit in Survey 4
5-19Y, A temp. at V
36.53 Degrees Celsius
Standard Deviation 0.510
36.55 Degrees Celsius
Standard Deviation 0.379
36.53 Degrees Celsius
Standard Deviation 0.570
36.61 Degrees Celsius
Standard Deviation 0.431
36.38 Degrees Celsius
Standard Deviation 0.430
Axillary Temperature at Visit in Survey 4
20+Y, A temp. at V
36.42 Degrees Celsius
Standard Deviation 0.444
36.68 Degrees Celsius
Standard Deviation 0.206
36.50 Degrees Celsius
Standard Deviation 0.000
36.39 Degrees Celsius
Standard Deviation 0.457

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were: Number of persons living in the same part of the house (PLSPH) among persons enrolled in the study (PES), in the following combinations: \< y/x (less than \[\<\] y PLSPH among x PES), y-z/x (y to z PLSPH among x PES), \> z/x (more than \[\>\] z PLSPH among x PES), y-z/\> x (y to z PLSPH among more than \[\>\] x PES), \> z/\> x (more than \[\>\] z PLSPH among more than \[\>\] x PES, or missing information). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, <3/1
34 Participants
13 Participants
3 Participants
2 Participants
78 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, >5/1
20 Participants
10 Participants
0 Participants
3 Participants
123 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, 4-5/2
106 Participants
49 Participants
13 Participants
36 Participants
737 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, <3/3
1 Participants
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, >5/3
13 Participants
7 Participants
4 Participants
1 Participants
45 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
1 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, Missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, <3/1
20 Participants
6 Participants
0 Participants
0 Participants
28 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, >5/2
111 Participants
38 Participants
10 Participants
34 Participants
560 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, 4-5/>3
1 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, >5/1
6 Participants
1 Participants
0 Participants
26 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, <3/2
22 Participants
2 Participants
2 Participants
234 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, 4-5/2
40 Participants
7 Participants
3 Participants
449 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, >5/2
33 Participants
7 Participants
6 Participants
575 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, 4-5/3
3 Participants
0 Participants
0 Participants
18 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, >5/>3
1 Participants
0 Participants
0 Participants
18 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, 4-5/1
32 Participants
15 Participants
1 Participants
2 Participants
146 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, >5/3
10 Participants
0 Participants
0 Participants
51 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, Missing
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, <3/2
46 Participants
14 Participants
6 Participants
14 Participants
280 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, >5/2
119 Participants
59 Participants
28 Participants
59 Participants
1038 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, 4-5/3
1 Participants
1 Participants
1 Participants
1 Participants
19 Participants
Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH/PES, >5/>3
1 Participants
2 Participants
1 Participants
1 Participants
9 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, 4-5/1
14 Participants
2 Participants
1 Participants
1 Participants
17 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, >5/1
8 Participants
3 Participants
1 Participants
0 Participants
37 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, <3/2
19 Participants
4 Participants
1 Participants
5 Participants
75 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, 4-5/2
76 Participants
13 Participants
9 Participants
17 Participants
357 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, <3/3
0 Participants
1 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, 4-5/3
10 Participants
1 Participants
0 Participants
0 Participants
14 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, >5/3
25 Participants
2 Participants
1 Participants
1 Participants
59 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH/PES, >5/>3
10 Participants
1 Participants
0 Participants
0 Participants
17 Participants
Number of Subjects Living in the Same House at Survey 1
5-19Y, Missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, <3/1
3 Participants
0 Participants
0 Participants
49 Participants
Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH/PES, 4-5/1
1 Participants
0 Participants
0 Participants
16 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were: Number of persons living in the same part of the house (PLSPH) among persons enrolled in the study (PES), in the following combinations: \< y/x (less than \[\<\] y PLSPH among x PES), y-z/x (y to z PLSPH among x PES), \> z/x (more than \[\>\] z PLSPH among x PES), y-z/\> x (y to z PLSPH among more than \[\>\] x PES), \> z/\> x (more than \[\>\] z PLSPH among more than \[\>\] x PES, or missing information). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, <3/1
27 Participants
18 Participants
8 Participants
2 Participants
59 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, 4-5/1
33 Participants
18 Participants
8 Participants
3 Participants
112 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, >5/2
76 Participants
32 Participants
19 Participants
27 Participants
1059 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, 4-5/3
0 Participants
0 Participants
0 Participants
0 Participants
11 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, >5/3
3 Participants
1 Participants
4 Participants
2 Participants
24 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, >5/>3
0 Participants
1 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, <3/1
34 Participants
3 Participants
1 Participants
3 Participants
23 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, 4-5/2
98 Participants
17 Participants
10 Participants
13 Participants
426 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, >5/2
105 Participants
28 Participants
15 Participants
17 Participants
548 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, >5/3
14 Participants
4 Participants
1 Participants
1 Participants
20 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, 4-5/3
0 Participants
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, >5/3
3 Participants
0 Participants
0 Participants
0 Participants
25 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, <3/3
1 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, >5/1
13 Participants
9 Participants
3 Participants
4 Participants
84 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, <3/2
37 Participants
21 Participants
8 Participants
14 Participants
306 Participants
Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH/PES, 4-5/2
93 Participants
48 Participants
17 Participants
24 Participants
964 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, 4-5/1
30 Participants
13 Participants
2 Participants
0 Participants
20 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, >5/1
16 Participants
3 Participants
0 Participants
0 Participants
38 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, <3/2
30 Participants
3 Participants
0 Participants
2 Participants
69 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, <3/3
2 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, 4-5/3
4 Participants
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH-PES, <3/1
14 Participants
0 Participants
0 Participants
0 Participants
40 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, 4-5/1
8 Participants
0 Participants
0 Participants
0 Participants
26 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, >5/1
5 Participants
0 Participants
1 Participants
0 Participants
51 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, <3/2
34 Participants
2 Participants
1 Participants
2 Participants
253 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, 4-5/2
39 Participants
3 Participants
0 Participants
2 Participants
553 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, >5/2
21 Participants
5 Participants
3 Participants
3 Participants
476 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
0 Participants
3 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were: Number of persons living in the same part of the house (PLSPH) among persons enrolled in the study (PES), in the following combinations: \< y/x (less than \[\<\] y PLSPH among x PES), y-z/x (y to z PLSPH among x PES), \> z/x (more than \[\>\] z PLSPH among x PES), y-z/\> x (y to z PLSPH among more than \[\>\] x PES), \> z/\> x (more than \[\>\] z PLSPH among more than \[\>\] x PES, or missing information). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, >5/2
75 Participants
44 Participants
19 Participants
26 Participants
984 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, 4-5/3
2 Participants
0 Participants
1 Participants
0 Participants
11 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, >5/3
6 Participants
11 Participants
1 Participants
2 Participants
29 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, <3/1
40 Participants
9 Participants
1 Participants
1 Participants
24 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, <3/2
24 Participants
13 Participants
0 Participants
2 Participants
88 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, 4-5/2
74 Participants
25 Participants
5 Participants
13 Participants
421 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, >5/2
103 Participants
36 Participants
7 Participants
15 Participants
507 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, 4-5/3
7 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, >5/3
30 Participants
2 Participants
0 Participants
0 Participants
17 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, <3/1
18 Participants
0 Participants
0 Participants
0 Participants
40 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, >5/2
28 Participants
6 Participants
2 Participants
3 Participants
463 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, >5/3
13 Participants
0 Participants
0 Participants
0 Participants
36 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, <3/1
31 Participants
16 Participants
7 Participants
11 Participants
63 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, 4-5/1
31 Participants
26 Participants
8 Participants
11 Participants
94 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, >5/1
15 Participants
10 Participants
6 Participants
2 Participants
94 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, <3/2
43 Participants
24 Participants
13 Participants
17 Participants
340 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, 4-5/2
76 Participants
30 Participants
19 Participants
22 Participants
973 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, 4-5/1
32 Participants
8 Participants
0 Participants
1 Participants
23 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, >5/1
31 Participants
1 Participants
0 Participants
3 Participants
42 Participants
Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, 4-5/1
7 Participants
0 Participants
0 Participants
0 Participants
27 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, >5/1
5 Participants
0 Participants
0 Participants
0 Participants
33 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, <3/2
43 Participants
3 Participants
0 Participants
1 Participants
273 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, 4-5/2
57 Participants
4 Participants
3 Participants
0 Participants
516 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, 4-5/3
0 Participants
0 Participants
0 Participants
0 Participants
14 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were: Number of persons living in the same part of the house (PLSPH) among persons enrolled in the study (PES), in the following combinations: \< y/x (less than \[\<\] y PLSPH among x PES), y-z/x (y to z PLSPH among x PES), \> z/x (more than \[\>\] z PLSPH among x PES), y-z/\> x (y to z PLSPH among more than \[\>\] x PES), \> z/\> x (more than \[\>\] z PLSPH among more than \[\>\] x PES, or missing information). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, >5/2
25 Participants
12 Participants
4 Participants
12 Participants
338 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, >5/3
42 Participants
9 Participants
3 Participants
1 Participants
38 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, >5/>3
5 Participants
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, <3/2
23 Participants
0 Participants
0 Participants
81 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, <3/3
1 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, 4-5/3
2 Participants
0 Participants
1 Participants
3 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, >5/3
11 Participants
1 Participants
0 Participants
67 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, >5/>3
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, <3/1
4 Participants
0 Participants
0 Participants
20 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, 4-5/1
4 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, >5/1
1 Participants
0 Participants
0 Participants
10 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, 4-5/2
26 Participants
2 Participants
0 Participants
119 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, >5/2
15 Participants
1 Participants
0 Participants
191 Participants
Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, <3/1
28 Participants
21 Participants
2 Participants
7 Participants
42 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, 4-5/1
24 Participants
14 Participants
4 Participants
5 Participants
74 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, >5/1
18 Participants
7 Participants
1 Participants
5 Participants
59 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, <3/2
27 Participants
18 Participants
3 Participants
10 Participants
74 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, 4-5/2
30 Participants
23 Participants
3 Participants
13 Participants
184 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH-PES, <3/3
0 Participants
0 Participants
1 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, 4-5/3
1 Participants
1 Participants
0 Participants
1 Participants
9 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, >5/3
14 Participants
7 Participants
2 Participants
1 Participants
62 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, 4-5/>3
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH/PES, >5/>3
1 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, <3/1
36 Participants
5 Participants
2 Participants
2 Participants
17 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, 4-5/1
35 Participants
11 Participants
1 Participants
2 Participants
23 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, >5/1
4 Participants
2 Participants
2 Participants
1 Participants
7 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, <3/2
13 Participants
5 Participants
2 Participants
0 Participants
10 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, 4-5/2
27 Participants
8 Participants
3 Participants
3 Participants
65 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, >5/2
31 Participants
10 Participants
3 Participants
4 Participants
149 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, <3/3
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH/PES, 4-5/3
5 Participants
1 Participants
0 Participants
0 Participants
12 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: the mean and standard deviation of the number of persons living in the same part of the house (PLSPH). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Subjects Living in the Same House at Survey 1
6M-4Y, PLSPH
6.4 Persons
Standard Deviation 4.83
6.3 Persons
Standard Deviation 4.23
6.5 Persons
Standard Deviation 3.98
5.8 Persons
Standard Deviation 2.14
6.5 Persons
Standard Deviation 4.28
Mean Number of Subjects Living in the Same House at Survey 1
5-19Y, PLSPH
6.9 Persons
Standard Deviation 4.55
6.6 Persons
Standard Deviation 3.53
5.9 Persons
Standard Deviation 1.91
6.5 Persons
Standard Deviation 3.04
7.1 Persons
Standard Deviation 4.69
Mean Number of Subjects Living in the Same House at Survey 1
20+Y, PLSPH
6.1 Persons
Standard Deviation 4.15
7.4 Persons
Standard Deviation 5.21
6.2 Persons
Standard Deviation 2.99
6.3 Persons
Standard Deviation 4.24

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: the mean and standard deviation of the number of persons living in the same part of the house (PLSPH). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Subjects Living in the Same House at Survey 2
6M-4Y, PLSPH
5.1 Persons
Standard Deviation 2.90
5.0 Persons
Standard Deviation 2.17
5.1 Persons
Standard Deviation 2.34
5.4 Persons
Standard Deviation 2.62
5.8 Persons
Standard Deviation 2.66
Mean Number of Subjects Living in the Same House at Survey 2
5-19Y, PLSPH
5.5 Persons
Standard Deviation 2.64
6.1 Persons
Standard Deviation 2.78
5.9 Persons
Standard Deviation 1.89
5.9 Persons
Standard Deviation 2.81
6.2 Persons
Standard Deviation 2.78
Mean Number of Subjects Living in the Same House at Survey 2
20+Y, PLSPH
4.7 Persons
Standard Deviation 3.35
6.5 Persons
Standard Deviation 3.24
7.8 Persons
Standard Deviation 3.27
5.3 Persons
Standard Deviation 2.56
5.4 Persons
Standard Deviation 2.64

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: the mean and standard deviation of the number of persons living in the same part of the house (PLSPH). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Subjects Living in the Same House at Survey 3
6M-4Y, PLSPH
5.1 Persons
Standard Deviation 2.73
5.4 Persons
Standard Deviation 2.74
5.1 Persons
Standard Deviation 3.40
5.0 Persons
Standard Deviation 2.43
5.6 Persons
Standard Deviation 2.48
Mean Number of Subjects Living in the Same House at Survey 3
5-19Y, PLSPH
5.9 Persons
Standard Deviation 3.25
5.1 Persons
Standard Deviation 2.04
5.5 Persons
Standard Deviation 1.85
5.8 Persons
Standard Deviation 2.06
6.0 Persons
Standard Deviation 2.42
Mean Number of Subjects Living in the Same House at Survey 3
20+Y, PLSPH
4.5 Persons
Standard Deviation 2.16
5.9 Persons
Standard Deviation 3.23
5.4 Persons
Standard Deviation 1.14
6.5 Persons
Standard Deviation 2.89
5.4 Persons
Standard Deviation 2.77

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: the mean and standard deviation of the number of persons living in the same part of the house (PLSPH). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Mean Number of Subjects Living in the Same House at Survey 4
6M-4Y, PLSPH
5.4 Persons
Standard Deviation 3.12
5.1 Persons
Standard Deviation 3.73
5.5 Persons
Standard Deviation 3.50
5.2 Persons
Standard Deviation 3.24
6.6 Persons
Standard Deviation 3.33
Mean Number of Subjects Living in the Same House at Survey 4
5-19Y, PLSPH
6.5 Persons
Standard Deviation 4.55
6.1 Persons
Standard Deviation 3.95
6.3 Persons
Standard Deviation 3.13
6.8 Persons
Standard Deviation 4.28
7.3 Persons
Standard Deviation 3.70
Mean Number of Subjects Living in the Same House at Survey 4
20+Y, PLSPH
5.0 Persons
Standard Deviation 2.94
6.3 Persons
Standard Deviation 2.22
5.0 Persons
Standard Deviation 0.00
6.6 Persons
Standard Deviation 3.96

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: localisation categories (i.e.: rural, urban, semi-rural or missing) and Type of Location (i.e.: Large city: \>1 million habitants; Small city: \>50000 \& \< 1 million habitants; Town: \> 10000 and \< 50000 habitants; Countryside: \< 10000 habitants or missing type of location). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, rural
309 Participants
136 Participants
45 Participants
106 Participants
1415 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, urban
39 Participants
22 Participants
10 Participants
11 Participants
803 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, semi-rural
25 Participants
12 Participants
3 Participants
2 Participants
262 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, missing - localisation
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, large city
18 Participants
14 Participants
7 Participants
7 Participants
355 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
18 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, town
44 Participants
16 Participants
5 Participants
6 Participants
644 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
6M-4Y, countryside
311 Participants
140 Participants
46 Participants
106 Participants
1463 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, rural
225 Participants
55 Participants
16 Participants
51 Participants
688 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, urban
50 Participants
13 Participants
4 Participants
5 Participants
350 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, semi-rural
19 Participants
3 Participants
3 Participants
2 Participants
128 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, missing - localisation
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, large city
25 Participants
5 Participants
4 Participants
4 Participants
162 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, small city
1 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, town
43 Participants
11 Participants
2 Participants
3 Participants
282 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, countryside
225 Participants
55 Participants
17 Participants
51 Participants
715 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
5-19Y, missing - type of localisation
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, rural
89 Participants
12 Participants
10 Participants
923 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, urban
26 Participants
3 Participants
0 Participants
370 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, semi-rural
4 Participants
2 Participants
1 Participants
147 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, missing - localisation
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, large city
16 Participants
3 Participants
0 Participants
181 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, small city
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, town
14 Participants
2 Participants
1 Participants
299 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, countryside
89 Participants
12 Participants
10 Participants
951 Participants
Number of Subjects by Localisation and Type of Location at Survey 1
20+Y, missing - type of localisation
0 Participants
0 Participants
0 Participants
1 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: localisation categories (i.e.: rural, urban, semi-rural) and Type of Location (i.e.: Large city: \>1 million habitants; Small city: \>50000 \& \< 1 million habitants; Town: \> 10000 and \< 50000 habitants; Countryside: \< 10000 habitants). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, large city
10 Participants
4 Participants
5 Participants
6 Participants
374 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, rural
212 Participants
120 Participants
51 Participants
60 Participants
1377 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, urban
44 Participants
16 Participants
14 Participants
15 Participants
995 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, semi-rural
27 Participants
12 Participants
2 Participants
1 Participants
251 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
6 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, town
34 Participants
12 Participants
9 Participants
9 Participants
632 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
6M-4Y, countryside
239 Participants
132 Participants
53 Participants
61 Participants
1611 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, rural
237 Participants
48 Participants
17 Participants
25 Participants
583 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, urban
72 Participants
22 Participants
11 Participants
10 Participants
472 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, semi-rural
24 Participants
1 Participants
1 Participants
1 Participants
103 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, large city
15 Participants
5 Participants
2 Participants
7 Participants
172 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, town
57 Participants
17 Participants
9 Participants
3 Participants
305 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
5-19Y, countryside
261 Participants
49 Participants
18 Participants
26 Participants
680 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, rural
94 Participants
6 Participants
2 Participants
6 Participants
769 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, urban
26 Participants
4 Participants
3 Participants
1 Participants
515 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, semi-rural
4 Participants
0 Participants
0 Participants
0 Participants
157 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, large city
6 Participants
2 Participants
0 Participants
1 Participants
191 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
5 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, town
20 Participants
2 Participants
3 Participants
0 Participants
330 Participants
Number of Subjects by Localisation and Type of Location at Survey 2
20+Y, countryside
98 Participants
6 Participants
2 Participants
6 Participants
915 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: localisation categories (i.e.: rural, urban, semi-rural) and Type of Location (i.e.: Large city: \>1 million habitants; Small city: \>50000 \& \< 1 million habitants; Town: \> 10000 and \< 50000 habitants; Countryside: \< 10000 habitants). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, rural
234 Participants
146 Participants
65 Participants
82 Participants
1531 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, urban
30 Participants
11 Participants
5 Participants
5 Participants
881 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, semi-rural
15 Participants
4 Participants
4 Participants
4 Participants
176 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, large city
7 Participants
3 Participants
1 Participants
3 Participants
386 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, town
23 Participants
9 Participants
4 Participants
2 Participants
541 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
6M-4Y, countryside
249 Participants
149 Participants
69 Participants
86 Participants
1659 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, rural
283 Participants
78 Participants
9 Participants
28 Participants
645 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, urban
42 Participants
12 Participants
4 Participants
7 Participants
404 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, semi-rural
16 Participants
4 Participants
0 Participants
0 Participants
80 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, large city
12 Participants
2 Participants
2 Participants
2 Participants
182 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, town
30 Participants
10 Participants
2 Participants
5 Participants
241 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
5-19Y, countryside
299 Participants
82 Participants
9 Participants
28 Participants
705 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, rural
147 Participants
8 Participants
5 Participants
3 Participants
868 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, urban
23 Participants
3 Participants
0 Participants
1 Participants
430 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, semi-rural
1 Participants
2 Participants
0 Participants
0 Participants
104 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, large city
15 Participants
0 Participants
0 Participants
0 Participants
185 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, town
8 Participants
3 Participants
0 Participants
1 Participants
273 Participants
Number of Subjects by Localisation and Type of Location at Survey 3
20+Y, countryside
148 Participants
10 Participants
5 Participants
3 Participants
943 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: localisation categories (i.e.: rural, urban, semi-rural) and Type of Location (i.e.: Large city: \>1 million habitants; Small city: \>50000 \& \< 1 million habitants; Town: \> 10000 and \< 50000 habitants; Countryside: \< 10000 habitants). Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, town
2 Participants
0 Participants
0 Participants
155 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, countryside
85 Participants
4 Participants
1 Participants
353 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, rural
153 Participants
102 Participants
20 Participants
53 Participants
536 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, urban
15 Participants
1 Participants
0 Participants
1 Participants
312 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, semi-rural
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, large city
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, town
15 Participants
1 Participants
0 Participants
1 Participants
311 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
6M-4Y, countryside
153 Participants
102 Participants
20 Participants
53 Participants
537 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, rural
184 Participants
49 Participants
14 Participants
11 Participants
186 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, urban
14 Participants
2 Participants
2 Participants
2 Participants
142 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, countryside
184 Participants
49 Participants
14 Participants
11 Participants
187 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, semi-rural
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, large city
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, small city
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
5-19Y, town
14 Participants
2 Participants
2 Participants
2 Participants
141 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, rural
85 Participants
4 Participants
1 Participants
352 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, urban
2 Participants
0 Participants
0 Participants
156 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, semi-rural
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, large city
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by Localisation and Type of Location at Survey 4
20+Y, small city
0 Participants
0 Participants
0 Participants
0 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main house construction material (MHCM) walls and MHCM floor. MHCM walls data were assessed for the following sub-categories: mud, brick, cement/plaster, cement/paint, other and missing. MHCM floor data were assessed for the following sub-categories: natural floor, rudimentary floor, parquet polished wood, vinyl or asphalt strips, ceramic tiles, cement, carpet, missing. Note: Natural floor = earth, sand, dung; Rudimentary floor = wood planks, palm, bamboo. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - natural floor
64 Participants
5 Participants
8 Participants
690 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - ceramic tiles
0 Participants
0 Participants
0 Participants
13 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - mud
43 Participants
7 Participants
9 Participants
548 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - brick
43 Participants
2 Participants
0 Participants
337 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - cement/plaster
12 Participants
5 Participants
1 Participants
192 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM walls - mud
97 Participants
62 Participants
34 Participants
84 Participants
869 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM walls - brick
190 Participants
76 Participants
12 Participants
12 Participants
504 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM walls - cement/plaster
41 Participants
16 Participants
7 Participants
11 Participants
383 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM walls - cement/paint
29 Participants
12 Participants
5 Participants
11 Participants
408 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM walls - other
16 Participants
4 Participants
0 Participants
1 Participants
316 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - natural floor
197 Participants
100 Participants
42 Participants
83 Participants
1079 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - ceramic tiles
0 Participants
1 Participants
0 Participants
0 Participants
30 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - cement
170 Participants
69 Participants
16 Participants
33 Participants
1309 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - cement
55 Participants
11 Participants
3 Participants
705 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
6M-4Y, MHCM floor - carpet
6 Participants
0 Participants
0 Participants
3 Participants
53 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM floor - carpet
0 Participants
1 Participants
0 Participants
27 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - mud
89 Participants
29 Participants
13 Participants
48 Participants
424 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - brick
119 Participants
23 Participants
3 Participants
4 Participants
223 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - cement/plaster
43 Participants
8 Participants
4 Participants
5 Participants
168 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - cement/paint
30 Participants
4 Participants
3 Participants
1 Participants
186 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - other
13 Participants
7 Participants
0 Participants
0 Participants
165 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM walls - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - natural floor
146 Participants
46 Participants
12 Participants
48 Participants
511 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - other
5 Participants
0 Participants
1 Participants
146 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - ceramic tiles
0 Participants
1 Participants
0 Participants
0 Participants
14 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - cement
146 Participants
24 Participants
11 Participants
10 Participants
607 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - carpet
2 Participants
0 Participants
0 Participants
0 Participants
30 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
5-19Y, MHCM floor - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 1
20+Y, MHCM walls - cement/paint
16 Participants
3 Participants
0 Participants
217 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main house construction material (MHCM) walls and MHCM floor. MHCM walls data were assessed for the following sub-categories: mud, brick, cement/plaster, cement/paint, other. MHCM floor data were assessed for the following sub-categories: natural floor, rudimentary floor, parquet polished wood, vinyl or asphalt strips, ceramic tiles, cement, carpet. Note: Natural floor = earth, sand, dung; Rudimentary floor = wood planks, palm, bamboo. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM walls - mud
49 Participants
30 Participants
15 Participants
29 Participants
1010 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - ceramic tiles
0 Participants
1 Participants
0 Participants
1 Participants
40 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - cement
84 Participants
50 Participants
20 Participants
22 Participants
1357 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM walls - mud
79 Participants
20 Participants
11 Participants
21 Participants
445 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM walls - brick
155 Participants
26 Participants
11 Participants
7 Participants
191 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM walls - cement/plaster
51 Participants
15 Participants
2 Participants
4 Participants
207 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM walls - cement/paint
34 Participants
5 Participants
1 Participants
0 Participants
182 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - rudimentary floor
1 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
1 Participants
0 Participants
5 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - carpet
5 Participants
0 Participants
1 Participants
0 Participants
58 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM walls - cement/plaster
33 Participants
14 Participants
8 Participants
8 Participants
472 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM walls - cement/paint
32 Participants
15 Participants
4 Participants
2 Participants
393 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM walls - other
6 Participants
8 Participants
6 Participants
6 Participants
290 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - natural floor
194 Participants
97 Participants
45 Participants
53 Participants
1145 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
1 Participants
0 Participants
6 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
15 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
6M-4Y, MHCM walls - brick
163 Participants
81 Participants
34 Participants
31 Participants
458 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM walls - other
14 Participants
5 Participants
4 Participants
4 Participants
133 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - natural floor
207 Participants
42 Participants
17 Participants
26 Participants
508 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
10 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - ceramic tiles
0 Participants
0 Participants
0 Participants
0 Participants
26 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - cement
117 Participants
29 Participants
11 Participants
9 Participants
587 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
5-19Y, MHCM floor - carpet
8 Participants
0 Participants
0 Participants
1 Participants
22 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM walls - mud
26 Participants
5 Participants
1 Participants
5 Participants
520 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM walls - brick
69 Participants
2 Participants
0 Participants
0 Participants
302 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM walls - cement/plaster
7 Participants
0 Participants
1 Participants
1 Participants
258 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM walls - cement/paint
15 Participants
0 Participants
0 Participants
0 Participants
215 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM walls - other
7 Participants
3 Participants
3 Participants
1 Participants
146 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - natural floor
88 Participants
7 Participants
2 Participants
5 Participants
653 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - parquet polished wood
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
1 Participants
0 Participants
4 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - ceramic tiles
1 Participants
0 Participants
0 Participants
0 Participants
15 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - cement
34 Participants
3 Participants
2 Participants
2 Participants
732 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 2
20+Y, MHCM floor - carpet
1 Participants
0 Participants
0 Participants
0 Participants
35 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main house construction material (MHCM) walls and MHCM floor. MHCM walls data were assessed for the following sub-categories: mud, brick, cement/plaster, cement/paint, other. MHCM floor data were assessed for the following sub-categories: natural floor, rudimentary floor, ceramic tiles, cement, carpet. Note: Natural floor = earth, sand, dung; Rudimentary floor = wood planks, palm, bamboo. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM walls - mud
65 Participants
42 Participants
19 Participants
33 Participants
969 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM walls - brick
143 Participants
91 Participants
41 Participants
43 Participants
485 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM walls - cement/plaster
23 Participants
10 Participants
10 Participants
5 Participants
350 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM walls - cement/paint
28 Participants
12 Participants
3 Participants
5 Participants
464 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM walls - other
20 Participants
6 Participants
1 Participants
5 Participants
320 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM floor - natural floor
188 Participants
111 Participants
54 Participants
65 Participants
1082 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM floor - ceramic tiles
1 Participants
0 Participants
0 Participants
0 Participants
26 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM floor - cement
85 Participants
49 Participants
20 Participants
25 Participants
1406 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
6M-4Y, MHCM floor - carpet
5 Participants
1 Participants
0 Participants
1 Participants
70 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM walls - mud
90 Participants
32 Participants
4 Participants
13 Participants
432 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM walls - brick
161 Participants
42 Participants
2 Participants
12 Participants
205 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM walls - cement/plaster
38 Participants
8 Participants
1 Participants
3 Participants
136 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM walls - cement/paint
41 Participants
5 Participants
2 Participants
2 Participants
214 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM walls - other
11 Participants
7 Participants
4 Participants
5 Participants
142 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM floor - natural floor
185 Participants
67 Participants
7 Participants
24 Participants
449 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM floor - rudimentary floor
0 Participants
1 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM floor - ceramic tiles
2 Participants
0 Participants
0 Participants
0 Participants
12 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM floor - cement
149 Participants
26 Participants
6 Participants
11 Participants
636 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
5-19Y, MHCM floor - carpet
5 Participants
0 Participants
0 Participants
0 Participants
32 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM walls - mud
46 Participants
3 Participants
4 Participants
3 Participants
520 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM walls - brick
90 Participants
4 Participants
0 Participants
0 Participants
298 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM walls - cement/plaster
10 Participants
0 Participants
1 Participants
0 Participants
188 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM walls - cement/paint
15 Participants
1 Participants
0 Participants
0 Participants
228 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM walls - other
10 Participants
5 Participants
0 Participants
1 Participants
168 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM floor - natural floor
124 Participants
9 Participants
4 Participants
3 Participants
651 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM floor - ceramic tiles
0 Participants
1 Participants
0 Participants
0 Participants
12 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM floor - cement
46 Participants
3 Participants
1 Participants
1 Participants
699 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 3
20+Y, MHCM floor - carpet
1 Participants
0 Participants
0 Participants
0 Participants
38 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main house construction material (MHCM) walls and MHCM floor. MHCM walls data were assessed for the following sub-categories: mud, brick, cement/plaster, cement/paint, other. MHCM floor data were assessed for the following sub-categories: natural floor, rudimentary floor, vinyl or asphalt strips, ceramic tiles, cement, carpet. Note: Natural floor = earth, sand, dung; Rudimentary floor = wood planks, palm, bamboo. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - ceramic tiles
0 Participants
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - carpet
4 Participants
0 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM walls - mud
33 Participants
14 Participants
2 Participants
14 Participants
127 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM walls - brick
92 Participants
76 Participants
17 Participants
33 Participants
231 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM walls - cement/plaster
23 Participants
8 Participants
1 Participants
2 Participants
120 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM walls - cement/paint
6 Participants
2 Participants
0 Participants
1 Participants
81 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM walls - other
14 Participants
3 Participants
0 Participants
4 Participants
289 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - natural floor
97 Participants
76 Participants
15 Participants
37 Participants
267 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - rudimentary floor
0 Participants
1 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - ceramic tiles
0 Participants
1 Participants
0 Participants
0 Participants
16 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - cement
70 Participants
23 Participants
5 Participants
16 Participants
541 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
6M-4Y, MHCM floor - carpet
1 Participants
2 Participants
0 Participants
1 Participants
22 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM walls - mud
40 Participants
4 Participants
0 Participants
2 Participants
36 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM walls - brick
114 Participants
27 Participants
9 Participants
5 Participants
78 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM walls - cement/plaster
24 Participants
11 Participants
4 Participants
1 Participants
52 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM walls - cement/paint
13 Participants
4 Participants
1 Participants
0 Participants
30 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM walls - other
7 Participants
5 Participants
2 Participants
5 Participants
132 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - natural floor
105 Participants
27 Participants
9 Participants
6 Participants
96 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM walls - other
3 Participants
1 Participants
0 Participants
153 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
5-19Y, MHCM floor - cement
89 Participants
24 Participants
7 Participants
7 Participants
214 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM walls - mud
18 Participants
0 Participants
1 Participants
76 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM walls - brick
52 Participants
1 Participants
0 Participants
171 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM walls - cement/plaster
13 Participants
2 Participants
0 Participants
70 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM walls - cement/paint
1 Participants
0 Participants
0 Participants
38 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - natural floor
50 Participants
1 Participants
0 Participants
201 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - rudimentary floor
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - vinyl/asphalt strips
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - ceramic tiles
0 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - cement
37 Participants
3 Participants
1 Participants
287 Participants
Number of Subjects by House Construction Material Regarding Walls and Floor at Survey 4
20+Y, MHCM floor - carpet
0 Participants
0 Participants
0 Participants
10 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: main house construction material (MHCM) roof, windows/eaves, nets. MHCM roof data were assessed for the following sub-categories: grass/palm, iron sheet, tiles, other, missing. MHCM windows/eaves data were assessed for the following sub-categories: closed, open, partially open, missing. MHCM nets data were assessed for the following sub-categories: nets not present, nets present on all windows, nets present on some windows, missing. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM, nets - present on all windows
26 Participants
6 Participants
1 Participants
21 Participants
450 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM windows/eaves - open
76 Participants
33 Participants
17 Participants
20 Participants
486 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM roof - grass/palm
112 Participants
53 Participants
22 Participants
44 Participants
453 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM roof - iron sheet
231 Participants
109 Participants
35 Participants
74 Participants
1980 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
7 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM roof - other
30 Participants
8 Participants
1 Participants
1 Participants
40 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM windows/eaves - closed
193 Participants
93 Participants
31 Participants
77 Participants
1467 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM windows/eaves - partially open
104 Participants
44 Participants
10 Participants
22 Participants
527 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM windows/eaves - missing
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM, nets - not present
322 Participants
157 Participants
54 Participants
91 Participants
1795 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
6M-4Y, MHCM, nets - present on some windows
25 Participants
7 Participants
3 Participants
7 Participants
235 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM roof - grass/palm
88 Participants
19 Participants
7 Participants
28 Participants
212 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM roof - iron sheet
193 Participants
48 Participants
16 Participants
30 Participants
944 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM roof - other
13 Participants
4 Participants
0 Participants
0 Participants
8 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM roof - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM windows/eaves - closed
154 Participants
44 Participants
14 Participants
38 Participants
669 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM windows/eaves - open
71 Participants
16 Participants
5 Participants
9 Participants
233 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM windows/eaves - partially open
69 Participants
11 Participants
4 Participants
11 Participants
264 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM windows/eaves - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM, nets - not present
256 Participants
63 Participants
21 Participants
42 Participants
853 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM, nets - present on all windows
22 Participants
6 Participants
1 Participants
11 Participants
197 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM, nets - present on some windows
16 Participants
2 Participants
1 Participants
5 Participants
116 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
5-19Y, MHCM, nets - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM roof - grass/palm
31 Participants
5 Participants
3 Participants
280 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM roof - iron sheet
84 Participants
12 Participants
8 Participants
1117 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
6 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM roof - other
4 Participants
0 Participants
0 Participants
37 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM roof - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM windows/eaves - closed
65 Participants
8 Participants
5 Participants
798 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM windows/eaves - open
25 Participants
5 Participants
2 Participants
291 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM windows/eaves - partially open
29 Participants
4 Participants
4 Participants
351 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM windows/eaves - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM, nets - not present
107 Participants
12 Participants
7 Participants
1081 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM, nets - present on all windows
8 Participants
3 Participants
2 Participants
223 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM, nets - present on some windows
4 Participants
2 Participants
2 Participants
136 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 1
20+Y, MHCM, nets - missing
0 Participants
0 Participants
0 Participants
1 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: main house construction material (MHCM) roof, windows/eaves, nets. MHCM roof data were assessed for the following sub-categories: grass/palm, iron sheet, tiles, other. MHCM windows/eaves data were assessed for the following sub-categories: closed, open, partially open. MHCM nets data were assessed for the following sub-categories: nets not present, nets present on all windows, nets present on some windows. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM roof - grass/palm
52 Participants
32 Participants
16 Participants
23 Participants
509 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM roof - iron sheet
201 Participants
102 Participants
46 Participants
50 Participants
2092 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM roof - other
30 Participants
14 Participants
5 Participants
3 Participants
21 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM windows/eaves - closed
97 Participants
54 Participants
30 Participants
39 Participants
1411 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM windows/eaves - open
88 Participants
45 Participants
20 Participants
19 Participants
669 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM windows/eaves - partially open
98 Participants
49 Participants
17 Participants
18 Participants
543 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM, nets - not present
242 Participants
136 Participants
62 Participants
66 Participants
1843 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM, nets - present on all windows
26 Participants
6 Participants
4 Participants
8 Participants
626 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
6M-4Y, MHCM, nets - present on some windows
15 Participants
6 Participants
1 Participants
2 Participants
154 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM roof - grass/palm
76 Participants
15 Participants
3 Participants
13 Participants
207 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM roof - iron sheet
241 Participants
54 Participants
26 Participants
23 Participants
940 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM roof - other
16 Participants
2 Participants
0 Participants
0 Participants
11 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM windows/eaves - closed
159 Participants
36 Participants
16 Participants
14 Participants
610 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM windows/eaves - open
85 Participants
24 Participants
6 Participants
17 Participants
294 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM windows/eaves - partially open
89 Participants
11 Participants
7 Participants
5 Participants
254 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM, nets - not present
290 Participants
65 Participants
23 Participants
28 Participants
793 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM, nets - present on all windows
36 Participants
5 Participants
3 Participants
6 Participants
296 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
5-19Y, MHCM, nets - present on some windows
7 Participants
1 Participants
3 Participants
2 Participants
69 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM roof - grass/palm
30 Participants
3 Participants
1 Participants
2 Participants
276 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM roof - iron sheet
80 Participants
7 Participants
4 Participants
5 Participants
1144 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM roof - tiles
1 Participants
0 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM roof - other
13 Participants
0 Participants
0 Participants
0 Participants
19 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM windows/eaves - closed
49 Participants
6 Participants
3 Participants
4 Participants
732 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM windows/eaves - open
42 Participants
3 Participants
2 Participants
2 Participants
372 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM windows/eaves - partially open
33 Participants
1 Participants
0 Participants
1 Participants
337 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM, nets - not present
115 Participants
9 Participants
3 Participants
4 Participants
1033 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM, nets - present on all windows
5 Participants
0 Participants
2 Participants
3 Participants
320 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 2
20+Y, MHCM, nets - present on some windows
4 Participants
1 Participants
0 Participants
0 Participants
88 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: main house construction material (MHCM) roof, windows/eaves, nets. MHCM roof data were assessed for the following sub-categories: grass/palm, iron sheet, tiles, other. MHCM windows/eaves data were assessed for the following sub-categories: closed, open, partially open. MHCM nets data were assessed for the following sub-categories: nets not present, nets present on all windows, nets present on some windows. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM roof - iron sheet
214 Participants
125 Participants
60 Participants
63 Participants
2111 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM roof - other
1 Participants
1 Participants
0 Participants
0 Participants
2 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM windows/eaves - partially open
10 Participants
2 Participants
0 Participants
0 Participants
204 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM, nets - not present
153 Participants
12 Participants
4 Participants
4 Participants
1052 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM, nets - present on all windows
11 Participants
0 Participants
0 Participants
0 Participants
262 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM, nets - present on some windows
7 Participants
1 Participants
1 Participants
0 Participants
88 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM windows/eaves - partially open
29 Participants
12 Participants
8 Participants
4 Participants
391 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM, nets - not present
244 Participants
149 Participants
63 Participants
84 Participants
1918 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM, nets - present on all windows
21 Participants
10 Participants
6 Participants
4 Participants
532 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM, nets - present on some windows
14 Participants
2 Participants
5 Participants
3 Participants
138 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM roof - grass/palm
76 Participants
16 Participants
1 Participants
5 Participants
186 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM roof - iron sheet
264 Participants
77 Participants
12 Participants
30 Participants
940 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM windows/eaves - closed
165 Participants
58 Participants
9 Participants
18 Participants
593 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM windows/eaves - open
143 Participants
26 Participants
2 Participants
16 Participants
357 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM windows/eaves - partially open
33 Participants
10 Participants
2 Participants
1 Participants
179 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM, nets - not present
290 Participants
83 Participants
13 Participants
28 Participants
818 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM, nets - present on all windows
31 Participants
9 Participants
0 Participants
4 Participants
261 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
5-19Y, MHCM, nets - present on some windows
20 Participants
2 Participants
0 Participants
3 Participants
50 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM roof - grass/palm
45 Participants
1 Participants
2 Participants
2 Participants
259 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM roof - iron sheet
123 Participants
12 Participants
3 Participants
2 Participants
1123 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM roof - other
3 Participants
0 Participants
0 Participants
0 Participants
11 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM windows/eaves - closed
112 Participants
9 Participants
4 Participants
1 Participants
715 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
20+Y, MHCM windows/eaves - open
49 Participants
2 Participants
1 Participants
3 Participants
483 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM roof - grass/palm
55 Participants
35 Participants
12 Participants
26 Participants
464 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM roof - tiles
0 Participants
0 Participants
0 Participants
1 Participants
9 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM roof - other
10 Participants
1 Participants
2 Participants
1 Participants
4 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM windows/eaves - closed
164 Participants
82 Participants
38 Participants
57 Participants
1352 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 3
6M-4Y, MHCM windows/eaves - open
86 Participants
67 Participants
28 Participants
30 Participants
845 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: main house construction material (MHCM) roof, windows/eaves, nets. MHCM roof data were assessed for the following sub-categories: grass/palm, iron sheet, other. MHCM windows/eaves data were assessed for the following sub-categories: closed, open, partially open. MHCM nets data were assessed for the following sub-categories: nets not present, nets present on all windows, nets present on some windows. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM roof - grass/palm
51 Participants
29 Participants
6 Participants
17 Participants
161 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM roof - iron sheet
111 Participants
67 Participants
14 Participants
28 Participants
673 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM windows/eaves - closed
124 Participants
58 Participants
13 Participants
34 Participants
725 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM windows/eaves - open
15 Participants
13 Participants
1 Participants
5 Participants
66 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM windows/eaves - partially open
29 Participants
32 Participants
6 Participants
15 Participants
57 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM, nets - present on all windows
8 Participants
1 Participants
2 Participants
2 Participants
79 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM roof - grass/palm
55 Participants
10 Participants
1 Participants
2 Participants
51 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM roof - iron sheet
134 Participants
37 Participants
13 Participants
9 Participants
276 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM windows/eaves - closed
139 Participants
32 Participants
11 Participants
9 Participants
292 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM windows/eaves - open
24 Participants
8 Participants
4 Participants
1 Participants
17 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM windows/eaves - partially open
35 Participants
11 Participants
1 Participants
3 Participants
19 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM, nets - not present
162 Participants
41 Participants
14 Participants
13 Participants
276 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM, nets - present on some windows
19 Participants
5 Participants
0 Participants
0 Participants
27 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM roof - grass/palm
27 Participants
0 Participants
1 Participants
98 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM roof - other
4 Participants
0 Participants
1 Participants
16 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM windows/eaves - closed
64 Participants
4 Participants
1 Participants
421 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM windows/eaves - open
9 Participants
0 Participants
0 Participants
33 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM windows/eaves - partially open
14 Participants
0 Participants
0 Participants
54 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM, nets - not present
74 Participants
4 Participants
1 Participants
438 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM, nets - present on all windows
7 Participants
0 Participants
0 Participants
32 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM roof - other
6 Participants
7 Participants
0 Participants
9 Participants
14 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM, nets - not present
156 Participants
95 Participants
16 Participants
51 Participants
712 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
6M-4Y, MHCM, nets - present on some windows
4 Participants
7 Participants
2 Participants
1 Participants
57 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM roof - other
9 Participants
4 Participants
2 Participants
2 Participants
1 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
5-19Y, MHCM, nets - present on all windows
17 Participants
5 Participants
2 Participants
0 Participants
25 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM roof - iron sheet
56 Participants
4 Participants
0 Participants
394 Participants
Number of Subjects Classified by House Construction Material Regarding Roof, Window/Eaves and Nets at Survey 4
20+Y, MHCM, nets - present on some windows
6 Participants
0 Participants
0 Participants
38 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main source of drinking water (MSDW): bottled water, closed water source (piped water, tube well, dug well, protected well), open water source (unprotected well, spring water, rainwater, tanker truck, surface water), missing; and Presence of electricity (PE): Yes, No, missing. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=786 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=258 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=81 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=188 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5088 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, MSDW - closed water source
182 Participants
41 Participants
13 Participants
19 Participants
767 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
6M-4Y, MSDW - bottled water
1 Participants
0 Participants
0 Participants
0 Participants
22 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
6M-4Y, MSDW - closed water source
246 Participants
111 Participants
28 Participants
49 Participants
1637 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
6M-4Y, MSDW - open water source
126 Participants
59 Participants
30 Participants
70 Participants
821 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, MSDW - open water source
111 Participants
30 Participants
10 Participants
39 Participants
390 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, MSDW - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, PE - Yes
48 Participants
13 Participants
4 Participants
4 Participants
384 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, PE - No
246 Participants
58 Participants
19 Participants
54 Participants
782 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, PE - missing
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, MSDW - bottled water
1 Participants
0 Participants
0 Participants
12 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, MSDW - closed water source
82 Participants
10 Participants
4 Participants
943 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, PE - No
101 Participants
12 Participants
10 Participants
1043 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, PE - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
6M-4Y, PE - Yes
66 Participants
24 Participants
7 Participants
13 Participants
780 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
6M-4Y, PE - No
307 Participants
146 Participants
51 Participants
106 Participants
1700 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
5-19Y, MSDW - bottled water
1 Participants
0 Participants
0 Participants
0 Participants
9 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, MSDW - open water source
36 Participants
7 Participants
7 Participants
485 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, MSDW - missing
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 1
20+Y, PE - Yes
18 Participants
5 Participants
1 Participants
397 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main source of drinking water (MSDW): bottled water, closed water source (piped water, tube well, dug well, protected well), open water source (unprotected well, spring water, rainwater, tanker truck, surface water); and Presence of electricity (PE): Yes, No. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=740 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=229 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=101 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=119 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5222 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
6M-4Y, MSDW - bottled water
1 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
6M-4Y, MSDW - closed water source
207 Participants
93 Participants
44 Participants
42 Participants
1784 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
6M-4Y, MSDW - open water source
75 Participants
55 Participants
23 Participants
34 Participants
835 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
6M-4Y, PE - Yes
49 Participants
18 Participants
9 Participants
9 Participants
824 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
6M-4Y, PE - No
234 Participants
130 Participants
58 Participants
67 Participants
1799 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
5-19Y, MSDW - bottled water
1 Participants
0 Participants
0 Participants
0 Participants
3 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
5-19Y, MSDW - closed water source
229 Participants
45 Participants
22 Participants
21 Participants
760 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
5-19Y, PE - No
273 Participants
59 Participants
18 Participants
32 Participants
792 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
20+Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
0 Participants
4 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
20+Y, PE - Yes
23 Participants
4 Participants
2 Participants
1 Participants
436 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
5-19Y, MSDW - open water source
103 Participants
26 Participants
7 Participants
15 Participants
395 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
5-19Y, PE - Yes
60 Participants
12 Participants
11 Participants
4 Participants
366 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
20+Y, MSDW - closed water source
87 Participants
7 Participants
4 Participants
1 Participants
987 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
20+Y, MSDW - open water source
37 Participants
3 Participants
1 Participants
6 Participants
450 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 2
20+Y, PE - No
101 Participants
6 Participants
3 Participants
6 Participants
1005 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main source of drinking water (MSDW): bottled water, closed water source (piped water, tube well, dug well, protected well), open water source (unprotected well, spring water, rainwater, tanker truck, surface water); and Presence of electricity (PE): Yes, No. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=791 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=268 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=92 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=130 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=5119 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
6M-4Y, MSDW - closed water source
185 Participants
97 Participants
37 Participants
53 Participants
1613 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
20+Y, MSDW - open water source
70 Participants
5 Participants
3 Participants
3 Participants
503 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
6M-4Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
1 Participants
26 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
6M-4Y, MSDW - open water source
94 Participants
64 Participants
37 Participants
37 Participants
949 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
6M-4Y, PE - Yes
36 Participants
25 Participants
8 Participants
11 Participants
775 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
6M-4Y, PE - No
243 Participants
136 Participants
66 Participants
80 Participants
1813 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
5-19Y, MSDW - bottled water
0 Participants
1 Participants
0 Participants
0 Participants
13 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
5-19Y, MSDW - closed water source
214 Participants
51 Participants
6 Participants
23 Participants
715 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
5-19Y, MSDW - open water source
127 Participants
42 Participants
7 Participants
12 Participants
401 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
5-19Y, PE - Yes
56 Participants
19 Participants
5 Participants
7 Participants
348 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
5-19Y, PE - No
285 Participants
75 Participants
8 Participants
28 Participants
781 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
20+Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
0 Participants
15 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
20+Y, MSDW - closed water source
101 Participants
8 Participants
2 Participants
1 Participants
884 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
20+Y, PE - Yes
19 Participants
3 Participants
0 Participants
1 Participants
386 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 3
20+Y, PE - No
152 Participants
10 Participants
5 Participants
3 Participants
1016 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention and risk factors characteristics were the following: Main source of drinking water (MSDW): bottled water, closed water source (piped water, tube well, dug well, protected well), open water source (unprotected well, spring water, rainwater, tanker truck, surface water); and Presence of electricity (PE): Yes, No. Data were collected across centers from subjects between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. Results were presented per the following P. falciparum parasite density status subgroups: Low, Medium, High, Very high, and Negative (Neg).

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=453 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=158 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=36 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=68 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
n=1684 Participants
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
6M-4Y, PE - No
148 Participants
98 Participants
20 Participants
51 Participants
464 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
5-19Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
0 Participants
0 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
6M-4Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
6M-4Y, MSDW - closed water source
139 Participants
79 Participants
15 Participants
38 Participants
656 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
6M-4Y, MSDW - open water source
29 Participants
24 Participants
5 Participants
16 Participants
191 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
6M-4Y, PE - Yes
20 Participants
5 Participants
0 Participants
3 Participants
384 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
5-19Y, MSDW - closed water source
155 Participants
38 Participants
12 Participants
9 Participants
247 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
5-19Y, MSDW - open water source
43 Participants
13 Participants
4 Participants
4 Participants
81 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
5-19Y, PE - Yes
23 Participants
8 Participants
3 Participants
4 Participants
161 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
5-19Y, PE - No
175 Participants
43 Participants
13 Participants
9 Participants
167 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
20+Y, MSDW - bottled water
0 Participants
0 Participants
0 Participants
1 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
20+Y, MSDW - closed water source
69 Participants
2 Participants
1 Participants
391 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
20+Y, MSDW - open water source
18 Participants
2 Participants
0 Participants
116 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
20+Y, PE - Yes
9 Participants
2 Participants
0 Participants
206 Participants
Number of Subjects Classified by House Information Regarding Main Source of the Drinking Water and Presence of Electricity at Survey 4
20+Y, PE - No
78 Participants
2 Participants
1 Participants
302 Participants

SECONDARY outcome

Timeframe: At each Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

The malaria prevention measures (MPM) data were collected across centers from subjects with age between and including: 6M-4Y, 5-19 Y and 20Y+, for each Survey. The MPM results include the following categories: Use of Mosquito coils over 7 days (UMc \> 7D), Use of Insecticide spray over 7 days (UIs \> 7D), Use of Commercial Repellents over 7 days (UCR \> 7D), Use of Traditional Repellents over 7 days (UTR \> 7D), Use of none of above over 7 days (Una \>7D), Use of indoor residual spray in past 12 months to spray interior walls (Uirs past 12M), Use of indoor residual spray - number of months ago (Uirs-nM) or Use of indoor residual spray- no spray (Uirs-no spray): the number of months ago for each Uirs-nM sub-categories is defined using the following \[x Months\]. Not all Uirs-nM sub-categories were analyzed in each survey.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=6401 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=6411 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6400 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=2399 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Una >7D, Yes
2663 Participants
2726 Participants
2778 Participants
905 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Una >7D, Missing/No
277 Participants
246 Participants
211 Participants
146 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs past 12M, Yes
59 Participants
15 Participants
7 Participants
3 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UMc > 7D, Yes
433 Participants
398 Participants
348 Participants
239 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UMc > 7D, Missing/No
2767 Participants
2799 Participants
2845 Participants
954 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UIs > 7D, Yes
101 Participants
60 Participants
48 Participants
27 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UIs > 7D, Missing/No
3099 Participants
3137 Participants
3145 Participants
1166 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UCR > 7D, Yes
4 Participants
5 Participants
24 Participants
20 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UCR > 7D, Missing/No
3196 Participants
3192 Participants
3169 Participants
1173 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UTR > 7D, Yes
7 Participants
9 Participants
0 Participants
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], UTR > 7D, Missing/No
3193 Participants
3188 Participants
3193 Participants
1191 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Una >7D, Missing/No
537 Participants
471 Participants
415 Participants
288 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs past 12M, Missing/No
3141 Participants
3182 Participants
3186 Participants
1190 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [1 Month]
9 Participants
1 Participants
1 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [11 Months]
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [12 Months]
5 Participants
1 Participants
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [10 Months]
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [2 Months]
6 Participants
3 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [3 Months]
21 Participants
5 Participants
3 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [4 Months]
9 Participants
2 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [5 Months]
1 Participants
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [6 Months]
6 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [7 Months]
1 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [9 Months]
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[6M-4Y], Uirs-nM [no spray]
3141 Participants
3182 Participants
3186 Participants
1190 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UMc > 7D, Yes
227 Participants
209 Participants
180 Participants
127 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UMc > 7D, Missing/No
1386 Participants
1418 Participants
1432 Participants
479 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UIs > 7D, Yes
45 Participants
32 Participants
20 Participants
10 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UIs > 7D, Missing/No
1568 Participants
1595 Participants
1592 Participants
596 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UCR > 7D, Yes
4 Participants
2 Participants
12 Participants
7 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UCR > 7D, Missing/No
1609 Participants
1625 Participants
1600 Participants
599 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UTR > 7D, Yes
3 Participants
3 Participants
0 Participants
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], UTR > 7D, Missing/No
1610 Participants
1624 Participants
1612 Participants
604 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Una >7D, Yes
1336 Participants
1381 Participants
1401 Participants
460 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs past 12M, Yes
24 Participants
8 Participants
3 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs past 12M, Missing/No
1589 Participants
1619 Participants
1609 Participants
605 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [1 Month]
2 Participants
1 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [11 Months]
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [12 Months]
2 Participants
1 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [2 Months]
1 Participants
2 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [3 Months]
13 Participants
3 Participants
0 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [4 Months]
2 Participants
0 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [5 Months]
0 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [6 Months]
4 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [7 Months]
0 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [9 Months]
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[5-19Y], Uirs-nM [no spray]
1589 Participants
1619 Participants
1609 Participants
605 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UMc > 7D, Yes
196 Participants
199 Participants
167 Participants
117 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UMc > 7D, Missing/No
1392 Participants
1388 Participants
1428 Participants
483 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UIs > 7D, Yes
46 Participants
30 Participants
28 Participants
11 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UIs > 7D, Missing/No
1542 Participants
1557 Participants
1567 Participants
589 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UCR > 7D, Yes
0 Participants
4 Participants
12 Participants
12 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UCR > 7D, Missing/No
1588 Participants
1583 Participants
1583 Participants
588 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UTR > 7D, Yes
4 Participants
4 Participants
0 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], UTR > 7D, Missing/No
1584 Participants
1583 Participants
1595 Participants
600 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Una >7D, Yes
1346 Participants
1350 Participants
1392 Participants
460 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Una >7D, Missing/No
242 Participants
237 Participants
203 Participants
140 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs past 12M, Yes
32 Participants
7 Participants
2 Participants
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs past 12M, Missing/No
1556 Participants
1580 Participants
1593 Participants
598 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [1 Month]
7 Participants
0 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [11 Months]
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [12 Months]
3 Participants
0 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [10 Months]
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [2 Months]
4 Participants
1 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [3 Months]
8 Participants
3 Participants
1 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [4 Months]
6 Participants
2 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [5 Months]
1 Participants
1 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [6 Months]
2 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [7 Months]
1 Participants
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [9 Months]
0 Participants
Number of Subjects With Malaria Prevention Measures (MPM) at Each Survey
[Y20+], Uirs-nM [no spray]
1556 Participants
1580 Participants
1593 Participants
598 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Data were collected across centers from subjects with age between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 1. The other Plasmodium species assessed were: P. Malaria, P. Vivax, P. Ovale. Infection were determined using a blood smear slide, and categorized according positive (Pos) and negative (Neg) results.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=3200 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=1613 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=1588 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Malariae, Pos
19 Participants
21 Participants
1 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Malariae, Neg
3181 Participants
1592 Participants
1587 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Vivax, Pos
0 Participants
0 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Vivax, Neg
3200 Participants
1613 Participants
1588 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Ovale, Pos
3 Participants
1 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 1
P.Ovale, Neg
3197 Participants
1612 Participants
1588 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Data were collected across centers from subjects with age between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 2. The other Plasmodium species assessed were: P. Malaria, P. Vivax, P. Ovale. Infection were determined using a blood smear slide, and categorized according positive (Pos) and negative (Neg) results.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=3197 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=1627 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=1587 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Ovale, Pos
6 Participants
3 Participants
2 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Ovale, Neg
3191 Participants
1624 Participants
1585 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Malariae, Pos
32 Participants
27 Participants
2 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Malariae, Neg
3165 Participants
1600 Participants
1585 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Vivax, Pos
0 Participants
0 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 2
P.Vivax, Neg
3197 Participants
1627 Participants
1587 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Data were collected across centers from subjects with age between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 3. The other Plasmodium species assessed were: P. Malaria, P. Vivax, P. Ovale. Infection were determined using a blood smear slide, and categorized according positive (Pos) and negative (Neg) results.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=3193 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=1612 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=1595 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Malariae, Pos
48 Participants
27 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Malariae, Neg
3145 Participants
1585 Participants
1595 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Vivax, Pos
0 Participants
0 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Vivax, Neg
3193 Participants
1612 Participants
1595 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Ovale, Pos
6 Participants
4 Participants
1 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 3
P.Ovale, Neg
3187 Participants
1608 Participants
1594 Participants

SECONDARY outcome

Timeframe: At Survey visit

Population: Analysis was performed on the According-to-Protocol (ATP) Cohort, which included all evaluable subjects for whom at least one laboratory result of blood sample was available at the survey visit.

Data were collected across centers from subjects with age between and including: 6M-4Y, 5-19 Y and 20Y+, for Survey 4. The other Plasmodium species assessed were: P. Malaria, P. Vivax, P. Ovale. Infection were determined using a blood smear slide, and categorized according positive (Pos) and negative (Neg) results.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=1193 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=606 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=600 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Malariae, Pos
32 Participants
28 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Malariae, Neg
1161 Participants
578 Participants
600 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Vivax, Pos
0 Participants
0 Participants
0 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Vivax, Neg
1193 Participants
606 Participants
600 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Ovale, Pos
3 Participants
3 Participants
1 Participants
Number of Subjects With Plasmodium Species Other Than P. Falciparum at Survey 4
P.Ovale, Neg
1190 Participants
603 Participants
599 Participants

SECONDARY outcome

Timeframe: At each Survey visit

Population: The analysis was performed on the Total cohort, which included all subjects enrolled in the study.

Serious adverse events (SAEs) assessed include medical occurrences that result in death, are life threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity. Capillary blood sampling was the only invasive procedure involved in this study. SAEs related to this procedure were recorded at the Survey visit.

Outcome measures

Outcome measures
Measure
Overall Study Group (Survey 1)
n=6404 Participants
Subjects at least 6 months of age at the time of Survey 1, conducted at Year 1 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 2)
n=6414 Participants
Subjects at least 6 months of age at the time of Survey 2, conducted at Year 2 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 3)
n=6400 Participants
Subjects at least 6 months of age at the time of Survey 3, conducted at Year 3 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Overall Study Group (Survey 4)
n=2400 Participants
Subjects at least 6 months of age at the time of Survey 4, conducted at Year 4 of the 4 annual cross sectional surveys performed preferably at peak transmission (end of rainy season), infected with P. falciparum parasite. Infection determined using a blood smear slide and determined using microscopy. Subjects were enrolled from the catchment areas of study 110021 (NCT00866619) but those who previously participated in study 110021 were excluded from this epidemiological study.
Neg PD Group (Survey 1)
Subjects from Survey 1 not infected with P.falciparum.
Number of Subjects With Serious Adverse Events (SAEs) Related to Study Procedure for Each Survey
0 Participants
0 Participants
0 Participants
0 Participants

Adverse Events

Overall Study Group (Survey 1)

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Overall Study Group (Survey 2)

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Overall Study Group (Survey 3)

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Overall Study Group (Survey 4)

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

GSK Response Center

GlaxoSmithKline

Phone: 866-435-7343

Results disclosure agreements

  • Principal investigator is a sponsor employee GSK agreements may vary with individual investigators, but will not prohibit any investigator from publishing. GSK supports the publication of results from all centers of a multi-center trial but requests that reports based on single-site data not precede the primary publication of the entire clinical trial.
  • Publication restrictions are in place

Restriction type: OTHER