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Metabolic Mechanisms Induced by Enteral DHA and ARA Supplementation in Preterm Infants

RecruitingNAAges any - 36 WeeksAllThe University of Texas Health Science Center at …
NCT05380401 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

A comprehensive analysis of the impact of exogenous enteral DHA and ARA supplementation on lipid metabolism including the production of downstream derived mediators and how this impacts important biological pathways such as metabolism, inflammation, and organogenic factors.

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📋 Eligibility rules (as published)
Inclusion Criteria: * born between 25 0/7 and 29 6/7 weeks of gestation * less than 48 hours of age at first lipid dose (The cohort is defined by gestational age rather than birth weight to avoid an over-represented sample of growth-restricted infants in birth weight defined cohorts.) Exclusion Criteria: * serious congenital anomalies * conditions at birth that will require surgery prior to discharge * imminent death such that withdrawal of intensive care support is anticipated within the first 72 hours after birth
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What it tests

  • Enfamil® DHA & ARA Supplement for Special Dietary Use
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Where

7 sites
University of California, Los Angeles (UCLA)
Los Angeles, United States
Yale New Haven Hospital
New Haven, United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, United States
Northwestern University
Chicago, United States
Weill Cornell Medicine
New York, United States
University Health System
San Antonio, United States
University of Texas Health Science Center at San Antonio
San Antonio, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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