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

ConditionPremature
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeUp to 36
SponsorThe University of Texas Health Science Center at San Antonio

About this trial

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.

Eligibility criteria

Qualifiers

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.)

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Enfamil® DHA & ARA Supplement for Special Dietary Use

Treatment groups

328 Participants
are divided into 4 treatment groups

Sponsors and collaborators

The University of Texas Health Science Center at San Antonio

Lead sponsor

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

Collaborator