About this trial
Growth-restricted very preterm infants (VPT) are born without adequate fat mass (FM) deposits and low docosahexaenoic acid (DHA) concentrations. They often experience further declines in DHA concentrations during the initial three weeks post-birth while advancing enteral feeds and receiving lipid supplementation predominantly through parenteral nutrition. These suboptimal enteral and parenteral nutrition practices significantly heighten the risk of faltering postnatal growth. One promising approach to mitigate these issues is enteral DHA supplementation. However, it remains unclear whether the early administration of DHA through enteral supplementation could lead to a more substantial increase in head growth without affecting FM accretion in growth-restricted VPT infants. To address this question, we propose a masked randomized clinical trial involving 152 VPT infants.
Eligibility criteria
Qualifiers
Gestational ages between 22 0/7 - 32 6/7 weeks gestation
< 25th centile birthweight
Disqualifiers
Major congenital/chromosomal anomalies
Terminal illness in which decisions to withhold or limit support have been made
Trial design
Treatments tested in this trial
- DHA
Treatment groups
Sponsors and collaborators
University of Alabama at Birmingham
Lead sponsor
Mead Johnson Nutrition
Collaborator