RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Metabolic Mechanisms Induced by Enteral Docosahexaenoic Acid (DHA) and Arachidonic Acid (ARA) Supplementation in Preterm Infants

Quick Facts

Study Start:2023-03-09
Study Completion:2028-04
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05380401

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:Not specified to 36 Weeks
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD
Inclusion CriteriaExclusion Criteria
  1. * born between 25 0/7 and 29 6/7 weeks of gestation
  2. * 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.)
  1. * serious congenital anomalies
  2. * conditions at birth that will require surgery prior to discharge
  3. * imminent death such that withdrawal of intensive care support is anticipated within the first 72 hours after birth

Contacts and Locations

Study Contact

Cynthia Blanco, MD, MSCI-TS
CONTACT
210-567-5225
blanco@uthscsa.edu
Diana Anzueto Guerra
CONTACT
210-567-5254
anzuetod@uthscsa.edu

Principal Investigator

Cynthia Blanco, MD, MSCI-TS
PRINCIPAL_INVESTIGATOR
University of Texas Health Science Center San Antonio

Study Locations (Sites)

University of California, Los Angeles (UCLA)
Los Angeles, California, 90404
United States
Yale New Haven Hospital
New Haven, Connecticut, 06511
United States
Ann & Robert H. Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611
United States
Northwestern University
Chicago, Illinois, 60611
United States
Weill Cornell Medicine
New York, New York, 10021
United States
University Health System
San Antonio, Texas, 78229
United States
University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center at San Antonio

  • Cynthia Blanco, MD, MSCI-TS, PRINCIPAL_INVESTIGATOR, University of Texas Health Science Center San Antonio

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-03-09
Study Completion Date2028-04

Study Record Updates

Study Start Date2023-03-09
Study Completion Date2028-04

Terms related to this study

Keywords Provided by Researchers

  • infant, premature
  • fatty acids
  • nutrition

Additional Relevant MeSH Terms

  • Premature