Coenzyme Q10 for Gulf War Illness: A Replication Study
NCT06515184 · Status: RECRUITING · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 192
Last updated 2026-05-01
Summary
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
- Gulf War Syndrome
- Persian Gulf Syndrome
- Mitochondrial Disorder, Respiratory Chain
Interventions
- DRUG
-
PharmaNord Bio-Quinone Active CoQ10 Gold 100mg
Each participant receives one softgel three times a day. Arm 1 receives one 100mg softgel and two placebo softgels per day. Because of the presence of the IND, the dropdown menu does not allow us to choose dietary supplement. The option "drug" was chosen as the closest permissible option.
- DRUG
-
PharmaNord Placebo
Each participant receives one softgel three times a day. Arm 3 receives three placebo softgels per day. Supplement is taken orally in divided doses, with the last softgel not close to bedtime. Because of the presence of the IND, the dropdown menu does not allow us to choose dietary supplement. The option "drug" was chosen as the closest permissible option.
- DRUG
-
PharmaNord Bio-Quinone Active CoQ10 Gold 100mg
Each participant receives one softgel three times a day. Arm 2 receives three 100mg softgels per day. Supplement is taken orally in divided doses, with the last softgel not close to bedtime. Because of the presence of the IND, the dropdown menu does not allow us to choose dietary supplement. The option "drug" was chosen as the closest permissible option.
Sponsors & Collaborators
-
United States Department of Defense
collaborator FED -
University of California, San Diego
lead OTHER
Principal Investigators
-
Beatrice A Golomb, MD, PhD · University of California, San Diego
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-09-13
- Primary Completion
- 2027-12-31
- Completion
- 2027-12-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Phase III Trial of Coenzyme Q10 in Mitochondrial Disease
NCT00432744 ·Status: COMPLETED ·Phase: PHASE3
-
Coenzyme Q10 as Treatment for Long Term COVID-19
NCT04960215 ·Status: COMPLETED ·Phase: PHASE2
-
UCSD Q10 and Aging Study
NCT02012322 ·Status: COMPLETED ·Phase: NA
-
Effects of Coenzyme Q10 Supplementation on Oxidative Stress, Antioxidant Capacity, Inflammatory Responses, Fatigue Elimination, and Exercise Performance in Athletes
NCT03321110 ·Status: COMPLETED ·Phase: NA
-
The Effects of Differing Cognitive Task Demands on Whole-body Energy Metabolism and Cerebral Blood-flow: Modulation by Multivitamins/Minerals and Coenzyme Q10
NCT02381964 ·Status: COMPLETED ·Phase: NA
-
Coenzyme Q-10 and Pulmonary Arterial Hypertension
NCT01148836 ·Status: COMPLETED ·Phase: NA
-
Nicotinamide Riboside Clinical Trial for GWI
NCT05243290 ·Status: RECRUITING ·Phase: NA
-
Effect of Endurance Training-Induced Coenzyme Q10 (CoQ10) Supplementation on Myokine, Exerkine Secretion and Cognitive Functions in Long-Distance Runners
NCT06619249 ·Status: RECRUITING ·Phase: PHASE4
-
Bioavailability and Impact of Coenzyme Q10 in Stressing Exercise in Senescence Athletes
NCT03893864 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy of Coenzyme Q10 Supplementation on Multi-Organ Dysfunction in Severely Burned Patients
NCT03968640 ·Status: WITHDRAWN ·Phase: PHASE3
-
Coenzyme Q10 Plus NADH Supplementation in Chronic Fatigue Syndrome/Myalgic Encephalomyelitis
NCT03186027 ·Status: COMPLETED ·Phase: NA
-
Effects of Coenzyme Q10 Supplement on Cardiovascular Risk Factors in Subjects at High Risk of Metabolic Syndrome
NCT06506630 ·Status: RECRUITING ·Phase: NA
-
Nutraceutical Support of Fatigue Reduction, Improved Physical, Mental & Cognitive Function and Mitochondrial Function
NCT04261881 ·Status: COMPLETED ·Phase: NA
-
Effect of CoQ10 on the Endocrine Function of Skeletal Muscle
NCT05412888 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Assessing Bioavailability of CoQ10 Supplementation in Burn Patients
NCT02251626 ·Status: UNKNOWN ·Phase: EARLY_PHASE1
-
Impact of Orally Administered BPM31510 on Mitochondrial Energetics in Older Adults With Sarcopenia
NCT04999488 ·Status: WITHDRAWN ·Phase: EARLY_PHASE1
-
Effectiveness of Qualia NAD+ Supplementation on Intracellular NAD Levels
NCT06505967 ·Status: RECRUITING ·Phase: NA
-
Effect of NMN Supplementation on Organ System Biology
NCT04571008 ·Status: COMPLETED ·Phase: NA
-
Pharmacokinetic Study on Three Formulations of Coenzyme Q10 With Different Carriers
NCT04035525 ·Status: UNKNOWN ·Phase: NA
-
Effect of "Nicotinamide Mononucleotide" (NMN) on Cardiometabolic Function
NCT03151239 ·Status: COMPLETED ·Phase: NA
-
The Efficacy of Oral Mitoquinone (MitoQ) Supplementation for Improving Physiological in Middle-aged and Older Adults
NCT02597023 ·Status: COMPLETED ·Phase: NA
-
Coenzyme Q10 in Older Athletes Treated With Statin Medications
NCT01026311 ·Status: COMPLETED ·Phase: PHASE4
-
Ca-Mg Butyrate in GWI
NCT05367245 ·Status: RECRUITING ·Phase: PHASE2
-
Clinical Trial to Measure the Maximun HR After ReConnect ® Supplementation vs. Placebo in CFS.
NCT02063126 ·Status: COMPLETED ·Phase: PHASE2/PHASE3
-
Bioavailability of Ubiquinone and Ubiquinol in Older Adults
NCT03020680 ·Status: COMPLETED ·Phase: PHASE1