Ubiquinol supplementation study Not Applicable
Conditions
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)
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
| Measure | Time frame |
|---|---|
| Total blood collected after two weeks of supplementation 1. CoQ10 Analysis 2. Routine blood parameters | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. DNA methylation patterns 2. mRNA expression in monocytes | — |
Countries
Germany
Outcome results
None listed