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Not listed Phase 3 Interventional

The RE-ENERGIZE Study: RandomizEd Trial of ENtERal Glutamine to minimIZE Thermal Injury

ClinicalTrials.gov ID: NCT00985205

Public ClinicalTrials.gov record NCT00985205. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:50 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Effects of Enteral Glutamine Supplementation on Mortality and Infectious Morbidity in Severely Burned Patients: a Multi-center Pilot Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to test the following hypotheses: 1. Enteral glutamine administration decreases in-hospital mortality in adult patients with severe thermal burn injuries. 2. Enteral glutamine administration decreases hospital-acquired blood stream infections from Gram negative organisms and length of stay in ICU and hospital for adult patients with severe thermal burn injuries. 3. Enteral glutamine administration will improve the physical function of surviving burn injured patients and reduce their cost of care. The objectives of this trial are to determine the overall treatment effect and safety of glutamine in burn patients. Specifically, the investigators want to assess the following outcomes in a sample of 1200 patients in 80 sites: 1. In patients with severe, life-threatening burn injury, what is the effect of enteral glutamine on time to discharge alive from hospital 2. In patients with severe, life-threatening burn injury, what is the effect of enteral glutamine on 6 month mortality, hospital-acquired blood stream infections from Gram negative organisms, hospital mortality, duration of stay in ICU and hospital, health-related quality of life, and health care resources?

Study identification

NCT ID
NCT00985205
Recruitment status
Not listed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Daren K. Heyland
Other
Enrollment
1,201 participants

Conditions and interventions

Conditions

Interventions

Dietary Supplement

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2010 (Actual)
Primary completion
Dec 2021 (Estimated)
Completion
Dec 2021 (Estimated)
Last update posted
Dec 30, 2021

2010 – 2021

United States locations

U.S. sites
27
U.S. states
19
U.S. cities
27
Facility City State ZIP Site status
University of South Alabama Medical Center Mobile Alabama 36609 —
Arizona Burn Center at Maricopa Medical Center Phoenix Arizona 85008 —
Southern California Regional Burn Ctr at LAC & USC Med. Ctr. Los Angeles California 90089-9235 —
Shriners Hospitals for Children Northern California Sacramento California 95817 —
Department of Anesthesiology, University of Colorado Aurora Colorado 80045 —
North Colorado Medical Center - Banner Health Greeley Colorado 80631 —
Connecticut Burn Center Bridgeport Connecticut 06610 —
The Burn Center at Washington Hospital Center Washington D.C. District of Columbia 20782 —
Shands Burn Center at the University of Florida Gainesville Florida 32610 —
University of South Florida/Tampa Gen. Hosp. Reg. Burn Center, FL Tampa Florida 33606 —
Joseph M Still Burn Center Augusta Georgia 30909 —
Department of Surgery University of Iowa Hospitals & Clinics Iowa City Iowa 52242 —
Mercy Hospital St. Louis St Louis Missouri 63141 —
CHI St.Elizabeth Regional Burn Center Lincoln Nebraska 68150 —
The Nebraska Medical Center Omaha Nebraska 68198-7835 —
Wake Forest University Health Sciences Winston-Salem North Carolina 27157 —
Akron's Children's Hospital, Paul & Carol David Foundation Akron Ohio 44308-1062 —
The Ohio State University Wexnar Medical Center Columbus Ohio 43210 —
Legacy Emmanuel Hospital & Health Center Portland Oregon 97232 —
The Western Pennsylvania Hospital Burn Center Pittsburgh Pennsylvania 15224 —
Firefighters' Regional Burn Center TN, University of Tennesse Health & Sciences Center Memphis Tennessee 38102 —
University of Texas Southwestern Dallas Texas 8563 —
JBSA Fort Sam Houston Fort Sam Houston Texas 78234-7767 —
University of Texas Medical Branch Galveston Texas 77555 —
Memorial Hermann/UTHSC Houston Texas 77030 —
Harbourview Medical Center Seattle Washington 98195-9796 —
Columbia-St. Mary's, Milwaukee, Wi Milwaukee Wisconsin 53202 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 26 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00985205, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 30, 2021 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00985205 live on ClinicalTrials.gov.

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