D-cycloserine: A Novel Treatment for Gulf War Illness (GWDCS)
Status unconfirmed · Phase 2 · Has a placebo group
Conditions studied: Gulf War Illness
In brief
The purpose of this study is to investigate the efficacy of d-cycloserine (DCS) treatment for Gulf War Illness (GWI). Gulf War veterans with Gulf War Illness experience numerous chronic health symptoms, including cognition and fatigue, which reduces their quality of life. Gulf War veterans are in urgent need of novel treatment plans to tackle elusive symptomatology of Gulf War Illness. By using the literature of previous studies, the investigators have chosen to investigate d-cycloserine as a possible candidate for treating GWI, specifically cognitive symptoms. DCS has been shown to reduce neuroinflammation, regulate glutamate levels, and improve synaptic functioning in key areas of the brain.
Key facts
- Study ID
- NCT02983734
- Run by
- Boston University Charles River Campus
- People needed
- 56
- Starts
- 2015-10-01
- Expected to finish
- 2019-09-01
- Last updated by the study team
- 2019-01-15
Who can join
Age: 43 and older, up to 85. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Veterans of the 1991 Gulf War, male or female
- Physical examination and laboratory findings within normal limits
- Willingness and ability to participate in the informed consent process and comply with study protocols
- Symptom criteria: Meets Gulf War Illness criteria with the cognitive symptom domain being present. Veteran does not have medical exclusions for Gulf War Illness
You may not qualify if…
- Veteran lacks the capacity to provide consent during the informed consent process
- Veteran has the one of the following medical exclusion conditions and/or has been active or received treatment within the past 5 years: Cancer (except nonmelanoma skin cancer), diabetes (not well managed), seizure disorder, heart disease (except hypertension), liver disease, kidney disease, Lupus, multiple sclerosis, stroke, chronic infectious disease, immune disorder/immunosuppression
- Veteran has a history of a major psychiatric or central nervous system disorder that can affect cognitive function (ie. epilepsy, brain tumor, Parkinson's Disease)
- Veteran has been hospitalized in the past 5 years for depression, PTSD, alcohol or drug dependence
- Veteran has current suicidal ideation or current alcohol or drug dependence
- Pregnant women, lactating women, women who are breastfeeding, or women of childbearing potential who are not using medically accepted forms of contraception
- Veteran is active duty personnel
Where it is running
- Boston University — Boston, Massachusetts, United States (enrolling)
Full record on ClinicalTrials.gov
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