Clinical Trials Directory

Trials / Completed

CompletedNCT06302023

Docosahexaenoic Acid (DHA) Supplementation During Pregnancy Reduces the Risk of Preterm Birth in Threatened Preterm Labor

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Khon Kaen University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to learn about the effects of Docosahexaenoic acid (DHA) in reducing the incidence of premature birth in threatened preterm labor The main questions it aims to answer are: * Can DHA supplementation reduce the incidence of premature birth in threatened preterm labor? * How does DHA supplementation affect pregnancy outcomes? Participants were organized into two groups * Group 1 (Intervention) Participants will be asked to take a DHA 1000mg per day * Group 2 (control) Participant will not need to take a DHA

Detailed description

Threatened preterm labor is defined as regular uterine contractions occurring before 37 completed weeks of gestation, without any cervical dilation.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTDocosahexaenoic acid (DHA) 1000 mgPregnant women will be ask to take a DHA 1000 mg per days at bedtime until delivery or 37 week of gestational age

Timeline

Start date
2024-04-01
Primary completion
2024-10-07
Completion
2024-10-07
First posted
2024-03-08
Last updated
2024-12-12

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT06302023. Inclusion in this directory is not an endorsement.