Trial Outcomes & Findings for Bloodsafe Ghana- Iron and Nutritional Counseling Strategy Pilot Study (NCT NCT04949165)

NCT ID: NCT04949165

Last Updated: 2024-07-31

Results Overview

Haemoglobin level at 4 months from the enrollment visit.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

223 participants

Primary outcome timeframe

4 months

Results posted on

2024-07-31

Participant Flow

Participant milestones

Participant milestones
Measure
Iron Supplementation
Iron Supplementation: low dose ferrous sulphate (65mg elemental iron) supplements
Control
Standard of care
Overall Study
STARTED
105
118
Overall Study
COMPLETED
74
56
Overall Study
NOT COMPLETED
31
62

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Bloodsafe Ghana- Iron and Nutritional Counseling Strategy Pilot Study

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Iron Supplementation
n=105 Participants
Iron Supplementation: low dose ferrous sulphate (65mg elemental iron) supplements
Control
n=118 Participants
Standard of care
Total
n=223 Participants
Total of all reporting groups
Age, Continuous
19.70 years
STANDARD_DEVIATION 2.51 • n=5 Participants
20.14 years
STANDARD_DEVIATION 3.09 • n=7 Participants
19.93 years
STANDARD_DEVIATION 2.83 • n=5 Participants
Sex: Female, Male
Female
79 Participants
n=5 Participants
61 Participants
n=7 Participants
140 Participants
n=5 Participants
Sex: Female, Male
Male
26 Participants
n=5 Participants
57 Participants
n=7 Participants
83 Participants
n=5 Participants
Race/Ethnicity, Customized
Akan
55 Participants
n=5 Participants
57 Participants
n=7 Participants
112 Participants
n=5 Participants
Race/Ethnicity, Customized
Ewe
16 Participants
n=5 Participants
28 Participants
n=7 Participants
44 Participants
n=5 Participants
Race/Ethnicity, Customized
Dagbani
1 Participants
n=5 Participants
2 Participants
n=7 Participants
3 Participants
n=5 Participants
Race/Ethnicity, Customized
Ga/Dangbe
26 Participants
n=5 Participants
19 Participants
n=7 Participants
45 Participants
n=5 Participants
Race/Ethnicity, Customized
Hausa
0 Participants
n=5 Participants
2 Participants
n=7 Participants
2 Participants
n=5 Participants
Race/Ethnicity, Customized
Other
7 Participants
n=5 Participants
10 Participants
n=7 Participants
17 Participants
n=5 Participants
Current student
No
3 Participants
n=5 Participants
2 Participants
n=7 Participants
5 Participants
n=5 Participants
Current student
Yes
102 Participants
n=5 Participants
116 Participants
n=7 Participants
218 Participants
n=5 Participants
National Blood Service Ghana deferral decision
Deferred
40 Participants
n=5 Participants
3 Participants
n=7 Participants
43 Participants
n=5 Participants
National Blood Service Ghana deferral decision
Not deferred
65 Participants
n=5 Participants
115 Participants
n=7 Participants
180 Participants
n=5 Participants
Haemoglobin from FBC (g/dL)
11.25 g/dL
STANDARD_DEVIATION 0.91 • n=5 Participants
13.39 g/dL
STANDARD_DEVIATION 1.26 • n=7 Participants
12.38 g/dL
STANDARD_DEVIATION 1.54 • n=5 Participants
Ferritin (log(ferritin + 1)
3.54 ug/L
STANDARD_DEVIATION 0.87 • n=5 Participants
4.21 ug/L
STANDARD_DEVIATION 0.67 • n=7 Participants
3.89 ug/L
STANDARD_DEVIATION 0.84 • n=5 Participants
History of blood loss in the last 3 months
No
78 Participants
n=5 Participants
78 Participants
n=7 Participants
156 Participants
n=5 Participants
History of blood loss in the last 3 months
Yes
27 Participants
n=5 Participants
40 Participants
n=7 Participants
67 Participants
n=5 Participants
Siblings with known related anaemia
No
104 Participants
n=5 Participants
117 Participants
n=7 Participants
221 Participants
n=5 Participants
Siblings with known related anaemia
Yes
1 Participants
n=5 Participants
1 Participants
n=7 Participants
2 Participants
n=5 Participants
Heavy, frequent or long duration periods among menstrating women
No
40 Participants
n=5 Participants
37 Participants
n=7 Participants
77 Participants
n=5 Participants
Heavy, frequent or long duration periods among menstrating women
Yes
37 Participants
n=5 Participants
25 Participants
n=7 Participants
62 Participants
n=5 Participants
Heavy, frequent or long duration periods among menstrating women
Not Applicable (Male or women who are no longer menstruating)
28 Participants
n=5 Participants
56 Participants
n=7 Participants
84 Participants
n=5 Participants
Body mass index (kg/mˆ2)
24.12 kg/mˆ2
STANDARD_DEVIATION 8.83 • n=5 Participants
23.07 kg/mˆ2
STANDARD_DEVIATION 3.31 • n=7 Participants
23.57 kg/mˆ2
STANDARD_DEVIATION 6.53 • n=5 Participants
Systolic blood pressure (mm Hg)
116.35 mm Hg
STANDARD_DEVIATION 10.76 • n=5 Participants
117.89 mm Hg
STANDARD_DEVIATION 11.08 • n=7 Participants
117.17 mm Hg
STANDARD_DEVIATION 10.93 • n=5 Participants
Diastolic blood pressure (mm Hg)
76.17 mm Hg
STANDARD_DEVIATION 7.94 • n=5 Participants
76.92 mm Hg
STANDARD_DEVIATION 9.13 • n=7 Participants
76.57 mm Hg
STANDARD_DEVIATION 8.58 • n=5 Participants
Number of meals yesterday
0 (fasting)
1 Participants
n=5 Participants
0 Participants
n=7 Participants
1 Participants
n=5 Participants
Number of meals yesterday
1 meal
10 Participants
n=5 Participants
6 Participants
n=7 Participants
16 Participants
n=5 Participants
Number of meals yesterday
2 meals
40 Participants
n=5 Participants
47 Participants
n=7 Participants
87 Participants
n=5 Participants
Number of meals yesterday
3 or more meals
54 Participants
n=5 Participants
65 Participants
n=7 Participants
119 Participants
n=5 Participants

PRIMARY outcome

Timeframe: 4 months

Haemoglobin level at 4 months from the enrollment visit.

Outcome measures

Outcome measures
Measure
Iron Supplementation
n=56 Participants
Iron Supplementation: low dose ferrous sulphate (65mg elemental iron) supplements
Control
n=74 Participants
Standard of care
Haemoglobin Level
11.35 g/dL
Standard Deviation 1.27
12.28 g/dL
Standard Deviation 1.46

Adverse Events

Iron Supplementation

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

Control

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

Protocol Manager for BLIS

University of Minnesota

Phone: (612)590-2697

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place