Old antibiotic tested as brain rescue for gulf war veterans
NCT ID NCT02983734
First seen Sep 09, 2026 · Last updated Sep 10, 2026 · Updated 1 time
Summary
Researchers are testing whether a daily pill of d-cycloserine can improve memory and mood in veterans of the 1991 Gulf War who have Gulf War Illness. The study enrolls 22 veterans with cognitive symptoms and assigns them to take either d-cycloserine or a placebo for four weeks. The drug is thought to calm brain inflammation and adjust glutamate, a chemical involved in memory. Participants complete memory tests and mood questionnaires to see if the drug makes a difference.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- d-cycloserine, an antibiotic drug repurposed to target brain inflammation and glutamate signaling
- What this could lead to
- If it works, d-cycloserine could become a treatment for the memory and thinking problems that many Gulf War veterans live with, and it might point to similar approaches for other conditions involving brain inflammation.
- What could go wrong
- This is a small Phase 2 trial with 22 participants, so any hint of benefit could be a chance result that does not hold up in larger studies. D-cycloserine can cause drowsiness, dizziness, or mood changes, and it may not help Gulf War Illness symptoms at all.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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22 people
The number who actually took part.
- Start date
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Oct 2015
- Finished
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Sep 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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43 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 Exclusion Criteria: * 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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Boston University
Boston, Massachusetts, 02215, United States
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Other studies related to the condition(s) this trial covers.
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