Mechanisms of Gulf War Illness

Status: Recruiting
Location: See location...
Intervention Type: Other, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Many veterans with Gulf War Illness developed chronic gastrointestinal symptoms during their deployment to the Persian Gulf. The pathophysiologic mechanisms of these chronic gastrointestinal symptoms are not well understood but cause significant morbidity in veterans. Our proposed studies will provide an innovative and novel treatment trial for chronic gastrointestinal symptoms in veterans with Gulf War Illness that were deployed into war zones. Given that there are currently no specific treatments for these disorders, and that current symptomatic approaches are far from ideal, proof of principle of our trial would be an extremely important advance as it would not only have a beneficial impact on the health of many thousands of our veterans, but also it would substantially reduce the many negative economic effects of this ailment on the VA Health Care System.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Veterans 18-65 years old with GWI and chronic GI symptoms (abdominal pain, diarrhea, bloating) that started during their deployment in the Persian Gulf

• Veterans 18-65 years old with GWI and chronic GI symptoms (abdominal pain, diarrhea, bloating)

• increased intestinal permeability on the lactulose/mannitol permeability test (ratio \>0.07)

• able and willing to cooperate with the study

Locations
United States
Tennessee
Memphis VA Medical Center, Memphis, TN
RECRUITING
Memphis
Contact Information
Primary
George N Verne
George.Verne@va.gov
(901) 523-8990
Backup
QiQi Zhou, MD PhD
qiqi.zhou@va.gov
(901) 523-8990
Time Frame
Start Date: 2023-10-16
Estimated Completion Date: 2027-07-31
Participants
Target number of participants: 80
Treatments
Experimental: Oral Glutamine
You will be asked to consume 5 grams of glutamine three times a day for 12 weeks. At week four, you will be asked to return to the CRC to be assessed, and then to return every four weeks until week 12, which will be the conclusion of the study.
Placebo_comparator: Whey Protein Powder
You will be asked to consume 5 grams of whey protein powder three times a day for 12 weeks. At week four, you will be asked to return to the CRC to be assessed, and then to return every four weeks until week 12, which will be the conclusion of the study.
Related Therapeutic Areas
Sponsors
Leads: VA Office of Research and Development

This content was sourced from clinicaltrials.gov