Actively Recruiting
Coenzyme Q10 for Gulf War Illness: A Replication Study
Led by University of California, San Diego · Updated on 2026-05-01
192
Participants Needed
1
Research Sites
167 weeks
Total Duration
On this page
Sponsors
U
University of California, San Diego
Lead Sponsor
U
United States Department of Defense
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this study is to assess whether a high quality preparation of ubiquinone (coenzyme Q10) benefits symptoms, function, and quality of life in veterans with Gulf War illness.
CONDITIONS
Official Title
Coenzyme Q10 for Gulf War Illness: A Replication Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Meets both CDC and Kansas deployment and symptom inclusion criteria
- Does not have a disqualifying condition
- Able to travel to a local Quest facility for study blood draws
- Adequate internet access to allow ZoomPro visit participation and remote survey completion
- Health prior to the Gulf War rated as "very good" or "excellent"
- Willing to defer initiation of discretionary treatments or supplements during the expected course of study participation
You will not qualify if you...
- Participating in another clinical trial
- Still-evolving adverse effects following another medication or health condition, such as covid or fluoroquinolone use
- On Coumadin/ warfarin
- Unable to participate for the required duration of the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UC San Diego
La Jolla, California, United States, 92093
Actively Recruiting
Research Team
J
Janis B Ritchie, BSN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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