Phase
Condition
Colic
Gastrointestinal Diseases And Disorders
Non-ulcer Dyspepsia (Nud)
Treatment
Control Arm
Oral Glutamine
Clinical Study ID
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
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
Exclusion
Exclusion Criteria:
current participation in another research protocol or unable to give informedconsent
women with a positive urine pregnancy test or breastfeeding
history of inflammatory bowel disease, lactose intolerance and/or celiac sprue
- hydrogen breath test for bacterial overgrowth
5.
- anti-endomysial antibody titer
use of NSAIDs 2 weeks before or during the study
known allergy to glutamine or whey protein
abdominal surgery except for removal of gallbladder, uterus, or appendix >6 monthsprior to entry into the study
Abnormal serum BUN and/or creatinine
Mannitol recovery out of the normal range of 5-25 U/g
history of kidney disease
allergies to monosodium glutamate
current use of anti-seizure medications
Study Design
Study Description
Connect with a study center
Memphis VA Medical Center, Memphis, TN
Memphis, Tennessee 38104-2127
United StatesActive - Recruiting
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