Clinical Trials Directory

Trials / Completed

CompletedNCT00115271

Antenatal Micronutrient Supplementation and Birth Weight

Maternal Micronutrient Supplementation to Reduce Low Birth Weight and Infant and Maternal Morbidity in Rural Nepal

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
5,000 (planned)
Sponsor
Johns Hopkins Bloomberg School of Public Health · Academic / Other
Sex
Female
Age
15 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this study was to determine the effects of providing supplements containing alternative combinations of micronutrients during pregnancy on birth weight and other infant and maternal health and nutritional outcomes in a rural area of Nepal.

Detailed description

Maternal micronutrient deficiencies are common in the developing world and may influence intrauterine growth and fetal and neonatal health and survival. Currently, policies for antenatal supplementation beyond iron-folic acid are not in place in these settings. And yet, the efficacy of such supplementation strategies has not been well established. Specifically, it is not clear if multiple micronutrient combinations will enhance fetal growth and newborn health and survival compared to single or smaller combinations of micronutrients. Also, while birth weight may serve as a proxy measure of newborn health, infant morbidity and mortality needs direct examination. Comparisons: Pregnant women received daily folic acid, folic acid plus iron, folic acid plus iron plus zinc, or a multiple micronutrient supplement containing 11 other nutrients all with vitamin A compared to a control group that received only vitamin A.

Conditions

Interventions

TypeNameDescription
DRUGNutritional supplements

Timeline

Start date
1999-01-01
Primary completion
2001-05-01
Completion
2001-05-01
First posted
2005-06-22
Last updated
2014-08-26

Source: ClinicalTrials.gov record NCT00115271. Inclusion in this directory is not an endorsement.