Mortality Clinical Trial
Official title:
Sex-Differential Health Interventions In Low-Birth-Weight Infants
NCT number | NCT00625482 |
Other study ID # | 2007-7041-121 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | February 2008 |
Verified date | April 2021 |
Source | Bandim Health Project |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Our group has consistently found that the major interventions to reduce morbidity and mortality in low-income countries have sex-differential effects. These interventions include BCG vaccine, oral polio vaccination (OPV), and vitamin A supplementation (VAS). Low-birth-weight (LBW) children constitute the largest high-risk group in low-income countries. According to current policy, they receive OPV at birth. Current evidence suggests that a policy of providing BCG with OPV for girls and VAS instead of OPV for boys at birth may improve survival in LBW neonates. This will be tested in a large randomized trial. We experienced an unexpected cluster of deaths among boys in the VAS arm, which could be due to chance, but we decided to stop randomizing boys to OPV or VAS. Very recent evidence has suggested that low-birth-weight boys may benefit from BCG at birth as well. Hence, we have obtained ethical permission to continue the trial with randomization of boys to OPV or OPV plus BCG.
Status | Completed |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | |
Gender | All |
Age group | N/A to 1 Month |
Eligibility | Inclusion Criteria: - Low-birth-weight infants (<2500 g) Exclusion Criteria: - Already received BCG/OPV - Overtly sick or have malformations at the time of enrolment - Clinical signs of vitamin A deficiency (very unlikely) |
Country | Name | City | State |
---|---|---|---|
Guinea-Bissau | Bandim Health Project | Bissau |
Lead Sponsor | Collaborator |
---|---|
Bandim Health Project | Danida, March of Dimes |
Guinea-Bissau,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Mortality | |||
Secondary | Overall severe morbidity as measured by number of hospitalizations | |||
Secondary | Morbidity due to rotavirus and malaria | |||
Secondary | Growth | |||
Secondary | BCG scar formation and PPD delayed type hypersensitivity (DTH) response | |||
Secondary | Changes in cytokine profile |
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