Glutamine Supplementation to Prevent Death or Infection in Extremely Premature Infants (Glutamine)
Infant, Newborn, Infant, Low Birth Weight, Infant, Small for Gestational Age
About this trial
This is an interventional treatment trial for Infant, Newborn focused on measuring NICHD Neonatal Research Network, Extremely Low Birth Weight (ELBW) infants, Prematurity, Glutamine, Total parenteral nutrition, Nutrition, Very low birth weight (VLBW) infants
Eligibility Criteria
Inclusion Criteria: 401-1000 gm More than 12 hrs and less than 72 hrs after birth; intravenous access Parental consent Exclusion Criteria: One or more major congenital anomalies Infants meeting criteria for terminal illness Congenital nonbacterial infection with overt signs at birth
Sites / Locations
- University of Alabama at Birmingham
- Stanford University
- University of California at San Diego
- Yale University
- University of Miami
- Emory University
- Indiana University
- Wayne State University
- University of New Mexico
- RTI International
- Cincinnati Children's Medical Center
- Case Western Reserve University, Rainbow Babies and Children's Hospital
- Brown University, Women & Infants Hospital of Rhode Island
- University of Texas Southwestern Medical Center at Dallas
- University of Texas Health Science Center at Houston
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Glutamine
Placebo
TrophAmine (B. Braun/McGaw) with cysteine hydrochloride (40mg/gm amino acids) with L-glutamine added (20% of the total amount of amino acids)
Standard TrophAmine (B. Braun/McGaw) with cysteine hydrochloride (40mg/gm amino acids)