Ca-Mg Butyrate in GWI

Recruiting Phase 2 Interventional Study
Gulf War Illness Chronic Fatigue Neurocognitive Dysfunction
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
40 – 70
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
120 (estimated)
Sponsor
VA Office of Research and Development · Federal
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About This Trial
The primary objective of this clinical trial is to determine if treatment with Butyrate formulation that consists of butyric acid as calcium and magnesium derivatives (Ca-Mg Butyrate) improves the physical function of men and women Veterans suffering from Gulf War Illness (GWI). The primary outcome measure is a change from baseline on the Short Form Health Survey 36-item (VSF-36), with respect to …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Gulf war era veteran deployed 40 and 70 years old, in good health by medical history prior to 1990 meeting GWI case definition of CDC and Kansas criteria and * currently have no exclusionary diagnoses (self- reported) that could reasonably explain the symptoms of their fatigui…
Contacts

Saurabh Chatterjee, PhD

(562) 826-8000

saurabhc@hs.uci.edu

CONTACT

Jonathan Skupsky

(562) 826-8000

Jonathan.Skupsky@va.gov

CONTACT