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Assessment of DHA On Reducing Early Preterm Birth — ADORE  

Preterm Birth Clinical Trial

Official title:
Assessment of DHA On Reducing Early Preterm Birth (ADORE Trial)

Clinical Trial Summary

The purpose of this study is to determine if giving a larger amount of DHA than currently included in some prenatal supplements can reduce early preterm birth (birth before 34 weeks of pregnancy).

Clinical Trial Description

Docosahexaenoic acid (DHA) is a nutrient found in some fish and eggs and its intake in US diets is typically low. Because DHA is important for early brain development, it has recently been added to many prenatal supplements. The usual amount is around 200 mg/day. Participants in this study are guaranteed to receive at least 200 mg/day of DHA. Almost 5 in 100 births in the US occur before 34 weeks of pregnancy. There is no way to predict which births will occur before 34 weeks. In an earlier study conducted at the University of Kansas Medical Center, women who received 600 mg DHA/day compared to no DHA had fewer births before 34 weeks of pregnancy with fewer complications of preterm birth. This study is designed to compare standard care (200 mg/day of DHA) to a higher amount of DHA (1000 mg/day) to determine if the higher amount will reduce early preterm birth (birth before 34 weeks of pregnancy). Individual participation in this study is expected last about 5 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02626299
Study type Interventional
Source University of Kansas Medical Center
Contact
Status Completed
Phase Phase 3
Start date June 8, 2016
Completion date October 5, 2020
View Details
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