← Eichor
Study identifier: NCT07699393 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pilot Study of Prenatal Choline Supplementation

Condition: Brain Development · Choline Nutrition  ·  Sponsor: Wayne State University

PhasePhase 2
Planned participants50
Who can joinAll sexes, 18 Years to 45 Years
Healthy volunteersYes

About this study

A double-blind, randomized, placebo-controlled trial (RCT; NCT04395196) of prenatal choline supplementation is ongoing (1) to assess the effectiveness of maternal choline supplementation during pregnancy to mitigate effects of PAE on three primary outcomes: infant recognition memory and postnatal growth restriction (weight and head circumference); (2) to assess the efficacy of this supplementation for mitigating alcohol effects on the following secondary outcomes: infant eyeblink conditioning, postnatal length, and information processing speed. The study design was based on a pilot feasibility study in 70 heavy-drinking pregnant women. Infants in the choline-treated arm were more likely to meet criterion for eyeblink conditioning than those in the placebo arm. Infants born to both the choline- and placebo-treated mothers were small at birth, but those in the choline arm showed considerable catch-up growth in weight and head circumference by 6.5 months, which persisted through 12 months. At 12 months, infants in the choline arm showed markedly better recognition memory compared to placebo-treated on the Fagan Test of Infant Intelligence, which is known to have predictive validity for school-age IQ. Of note, infants with heavy prenatal alcohol exposure whose mothers were in the active choline treatment arm performed better on FTII novelty preference neurobehavioral testing than infants in an observational study that was running in parallel who had no prenatal alcohol exposure. …

This description comes directly from the study's public registry record.

Talk to the study team

R. Colin Carter, MD, MMSc  ·  +12123052995  ·  rcc2142@cumc.columbia.edu

Sandra W Jacobson, PhD  ·  +13139935454  ·  sandra.jacobson@wayne.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Cape TownCape Town, South AfricaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07699393