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Last Updated: December 11, 2019

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CLINICAL TRIALS PROFILE FOR UBIQUINOL

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Clinical Trials for Ubiquinol

Trial ID Title Status Sponsor Phase Summary
NCT00891917 Liq-NOL Efficacy in Pediatric Patients With Down Syndrome Completed Children's Hospital Medical Center, Cincinnati Phase 2 The purpose of this study is to measure the effects of LiQ-NOL supplementation on language production using the Clinical Evaluation of Language Fundamentals test, language sampling using the mean length of utterance test, and speech articulation using the Goldman-Fristoe Test of Articulation.
NCT01702987 Evaluation of Ubiquinol on Mitochondrial Oxidative Capacity in Statin Patients Using 31PMRS Completed Beth Israel Deaconess Medical Center N/A It is our primary hypothesis that statin drugs impair skeletal muscle mitochondrial function and that ubiquinol (the reduced active form of CoQ10) supplementation will block impairment of PCr recovery kinetics in patients using statins. The investigators propose a pilot study to extend our research to examine PCr recovery kinetics in 20 statin users randomized in a parallel arm study to either ubiquinol or placebo over 4 weeks.
NCT01872351 Therapy for Chronic Fatigue Syndrome: A Presumptive Mitochondrial Disorder Withdrawn Columbia University Phase 1 The purpose of this study is to determine whether therapy that has been shown to be beneficial for mitochondrial diseases is also beneficial for Chronic Fatigue Syndrome (CFS) patients. This study is a chart review of previous CFS patients who received daily conditioning exercise, a high protein diet and nutraceutical therapy (ENT). Prescribed nutraceutical supplements included alpha-lipoic acid, acetyl-L-carnitine, omega-3fatty acids (maxDHA), coenzyme Q10 (CoQ10), plus a multivitamin. Twelve CFS male and female patients between the ages of 20-70 years will be recruited to participate in this pilot study. Subjects will be eligible to participate if they meet the criteria for CFS of the Centers for Disease Control and Prevention (CDC). These include persistent, unexplained fatigue for at least 6 months, concurrent with four of the following: impaired memory/concentration, sore throat, new headaches, unrefreshing sleep, muscle pain, multi-joint pain, tender lymph nodes, and post-exertional malaise.
NCT01948063 Ubiquinol (Reduced COQ10) for Patients With Sepsis Completed Kaneka Pharma America LLC Phase 2 This study aims to determine if Ubiquinol (reduced form of COQ10) will attenuate mitochondrial injury and decrease inflammatory response in patients suffering from sepsis.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for Ubiquinol

Condition Name

Condition Name for
Intervention Trials
Hypercholesterolemia 1
Sepsis 1
Chronic Fatigue Syndrome 1
HMG COA Reductase Inhibitor Adverse Reaction 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Syndrome 2
Heart Failure 2
Mitochondrial Diseases 2
Fatigue 2
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Clinical Trial Locations for Ubiquinol

Trials by Country

Trials by Country for
Location Trials
United States 11
Pakistan 1
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Trials by US State

Trials by US State for
Location Trials
Massachusetts 4
New York 2
Kansas 1
Minnesota 1
Florida 1
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Clinical Trial Progress for Ubiquinol

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 4 1
Phase 3 1
Phase 2 5
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Not yet recruiting 4
Completed 3
Recruiting 3
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Clinical Trial Sponsors for Ubiquinol

Sponsor Name

Sponsor Name for
Sponsor Trials
Beth Israel Deaconess Medical Center 3
Kaneka Pharma America LLC 2
University of Kansas Medical Center 1
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Sponsor Type

Sponsor Type for
Sponsor Trials
Other 9
Industry 3
U.S. Fed 1
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