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Postnatal Choline Supplementation in Children With Prenatal Alcohol Exposure

Fetal Alcohol Spectrum Disorders Clinical Trial

Official title:
Postnatal Choline Supplementation in Children With Prenatal Alcohol Exposure

Clinical Trial Summary

The purpose of this study is to determine if choline bitartrate can be administered daily to children with prenatal alcohol exposure, ages 2.5 to 5, as a potential treatment for brain development and cognitive functioning.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01149538
Study type Interventional
Source University of Minnesota - Clinical and Translational Science Institute
Contact
Status Completed
Phase Phase 1/Phase 2
Start date July 2010
Completion date September 2014
View Details
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