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A Randomised, Double-Blind, Placebo-Controlled Trial of the Effects of Selenium Supplementation on Pregnancy Outcome and Disease Progression in HIV-Infected Pregnant Women in Lagos, Nigeria

Phase 3
Conditions
HIV/AIDS
Pregnancy and Childbirth
Registration Number
PACTR201809756724274
Lead Sponsor
College of Medicine University of Lagos
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
180
Inclusion Criteria

1. Pregnant women aged 15 to 49 years
2. Singleton gestation at 14 to 26 weeks’ gestation
3. On antiretroviral treatment (ART) for at least 3 months prior to enrolment.

Exclusion Criteria

1. Multiple Gestations
2. Significant renal and hepatic impairment
3. An expected delivery date beyond March 2019
4. Mid-trimester pregnancy loss in the index pregnancy
5. Receipt of a long course of a mineral supplement containing selenium during the 6 months prior to enrolment
6. Refusal of consent at enrolment or withdrawal of consent during the study
7. Failure to receive the study intervention (selenium or placebo) for a cumulative period of at least 8 weeks before delivery.
8. To be excluded in the final analysis of the primary end-points (see below) are women who delivered by Caesarean section or those who had iatrogenic preterm delivery.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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