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.
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