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Determination of effects of Coenzyme Q10 or ubiquinol in human gene expression and related physiological readouts

Ubiquinol supplementation in humans: a proof of principle study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN26780329
Enrollment
53
Registered
2012-06-29
Start date
2009-01-01
Completion date
Unknown
Last updated
2017-11-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ubiquinol supplementation study Not Applicable

Interventions

Ubiquinol supplementation, all participants got the same treatment: 150 mg Q10H2 daily in the form of three softgel capsules (50 mg) with each principal meal for 14 days.

Sponsors

Kaneka Corporation (Japan)
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Age >17 years 2. Gender: Male 3. No history of gastrointestinal, hepatic, cardiovascular or renal diseases 4. A habit of non- or occasional smoking and maintenance of usual nutrition habits

Exclusion criteria

Exclusion criteria: 1. Age <17 years 2. Gender: Female 3. History of gastrointestinal, hepatic, cardiovascular or renal diseases, smoking, eating disorders

Design outcomes

Primary

MeasureTime frame
Total blood collected after two weeks of supplementation 1. CoQ10 Analysis 2. Routine blood parameters

Secondary

MeasureTime frame
1. DNA methylation patterns 2. mRNA expression in monocytes

Countries

Germany

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 25, 2026