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NCT05380401 · ClinicalTrials.gov registry record · NA
Metabolic Mechanisms Induced by Enteral DHA and ARA Supplementation in Preterm Infants
A NA study of Premature, sponsored by The University of Texas Health Science Center at San Antonio.
- Recruiting
- Registry status
- NA
- Development phase
- 328
- Enrollment target
- 7
- Study locations
NCT05380401 is a NA study of Premature that is actively recruiting participants, run by The University of Texas Health Science Center at San Antonio. The registered enrollment target is 328 participants, above the 153-participant average among 4 other Premature trials with a reported enrollment target (114% higher). The trial reports 7 study locations across 5 states.
The verdict
NCT05380401, a NA study of Premature, is actively recruiting participants, sponsored by The University of Texas Health Science Center at San Antonio.
- RECRUITING
- Registry status
- NA
- Development phase
- 328 participants
- Enrollment target
- 7
- Study locations
Study Summary
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.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Enfamil® DHA & ARA Supplement for Special Dietary Use
Study Locations (7)
Illinois
- Ann & Robert H. Lurie Children's Hospital of Chicago - Chicago
- Northwestern University - Chicago
Texas
- University Health System - San Antonio
- University of Texas Health Science Center at San Antonio - San Antonio
California
- University of California, Los Angeles (UCLA) - Los Angeles
Connecticut
- Yale New Haven Hospital - New Haven
New York
- Weill Cornell Medicine - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 328 participants |
| Start Date | 2023-03-09 |
| Est. Completion | 2028-04 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05380401
The ClinicalTrials.gov registry entry for NCT05380401 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 328 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 153-participant average among 4 other Premature trials with a reported enrollment target (114% higher). The listed sponsor is The University of Texas Health Science Center at San Antonio, which has 378 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Premature appearing as the primary indexed condition, and to 1 intervention - of which Enfamil® DHA & ARA Supplement for Special Dietary Use is the first listed.
NCT05380401 reports 7 study locations spanning 5 distinct geographic areas - top geographies include Illinois, Texas, California.
Frequently Asked Questions
What is clinical trial NCT05380401 about?
NCT05380401 is a clinical study titled "Metabolic Mechanisms Induced by Enteral DHA and ARA Supplementation in Preterm Infants". 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.
What is the current status of trial NCT05380401?
This trial is currently recruiting. It is a NA study. The enrollment target is 328 participants. The study started on 2023-03-09. Estimated completion is 2028-04.
What conditions does trial NCT05380401 study?
This clinical trial studies the following conditions: Premature.
What interventions are being tested in trial NCT05380401?
The interventions under investigation include: Enfamil® DHA & ARA Supplement for Special Dietary Use (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT05380401?
This trial is sponsored by The University of Texas Health Science Center at San Antonio, which has 378 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05380401 being conducted?
This trial has 7 study locations across California, Connecticut, Illinois, New York, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.