Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 1:49 PM
Ignite Modification Date:
2025-12-24 @ 1:49 PM
NCT ID:
NCT04069195
Eligibility Criteria:
Inclusion Criteria:
* regnant female military health care beneficiaries ≥18 years of age
* Between the 8th and 14th week of pregnancy at enrollment
* BMI of ≥30.0 kg/m2 and/or history of previous preterm delivery at \<36 weeks gestation
* Planning to deliver at WRNMMC
* DEERS-eligible
* All infants born to mothers enrolled in this study who do not meet any exclusion criteria
Exclusion Criteria:
* Routine use of DHA supplement (including DHA containing prenatal vitamins) and/or fish consumption greater than twice per week
* Women with a fish allergy
* Known major fetal anomaly believed to be lethal
* Maternal treatment for clotting disorder
* Allergy to corn or soybean oils
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT04069195
Study Brief:
Protocol Section:
NCT04069195