Group B Streptococcal Carrier State Prevalence Among Arab Pregnant Women in Northern Israel District
NCT ID: NCT02528890
Last Updated: 2016-04-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
196 participants
OBSERVATIONAL
2015-09-30
2016-03-31
Brief Summary
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Detailed Description
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In order to prevent early onset GBS infection of the newborn, pregnant women are treated with preventive antibiotics during labor based on either of two protocols:
A. Risk factors: Women with risk factors such as premature birth, prolonged premature rupture of membranes, intra-partum maternal fever or a previous child with GBS infection are treated.
B. Universal screening: Towards the end of pregnancy, at 35 - 37th week, a vaginal/anal swab for GBS is taken, and those found positive will be treated.
According to the Israeli Ministry of Health regulations' from July 2005 it is not accepted to routinely perform screening for GBS in pregnant women at 35-37th week of pregnancy. Therefore, the Israeli approach to prevent early neonatal GBS infection is based mainly on antibiotic prophylaxis treatment during labor of all pregnant women with risk factors.
In a study conducted at the Western Galilee Medical Center in the city of Nahariya and published in 2006, there was a significant increase in the GBS carrier state rate compared to previously published studies. It was also found that higher GBS carrier state rates prevail among Arab women compared to Jewish women.
The primary question of this study is to calculate GBS carrier state prevalence among pregnant Arab women attending the labor ward at the Nazareth Hospital at the 34 to 40th week of their pregnancy.
A vaginal / anal swab will be taken from all eligible participants to identify GBS carriers by PCR (polymerase chain reaction) test.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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preganat women between 34 - 40 weeks
Eligible pregnant women, who meet the inclusion criteria, will have a vaginal/anal swab taken to identify positive GBS carriers by PCR (polymerase chain reaction) test.
vaginal/anal swab for GBS from all participants
All eligible pregnant women, who meet the inclusion criteria and gave their informed consent to participate in the study has to complete a questionnaire and have a vaginal / anal swab taken to identify positive GBS carriers by PCR (polymerase chain reaction) test.
Interventions
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vaginal/anal swab for GBS from all participants
All eligible pregnant women, who meet the inclusion criteria and gave their informed consent to participate in the study has to complete a questionnaire and have a vaginal / anal swab taken to identify positive GBS carriers by PCR (polymerase chain reaction) test.
Eligibility Criteria
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Inclusion Criteria
2. Origin: Arab
3. Gestational age: 34 to 40
Exclusion Criteria
2. Women in active labor who has had one or more vaginal examinations.
18 Years
40 Years
FEMALE
No
Sponsors
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The Nazareth Hospital, Israel
OTHER
Responsible Party
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Marwan Hakim
Dr.
Principal Investigators
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Marwan M Hakim, MD, DSc
Role: PRINCIPAL_INVESTIGATOR
Nazareth Hospital EMMS
Locations
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Nazareth Hospital
Nazareth, , Israel
Countries
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Other Identifiers
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15-2015
Identifier Type: -
Identifier Source: org_study_id
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