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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04098510
Other study ID # MitoQ
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 8, 2019
Est. completion date September 30, 2020

Study information

Verified date September 2019
Source University of Copenhagen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine mitoquinone mesylate concentration levels in skeletal muscle samples obtained after intake of an acute oral dose of MitoQ.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date September 30, 2020
Est. primary completion date September 30, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Healthy,

- Male

- 18-40 years of age

Exclusion Criteria:

- Previous use of MitoQ or CoQ-10 within 30 days of screening appointment

- Ongoing use of MitoQ

- Smoking

- Ongoing treatment with medications

- Disease deemed by the MD to infer a risk to participate in the trial

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
MitoQ
Subjects ingest 8x20 mg MitoQ capsules

Locations

Country Name City State
Denmark August Krogh Building Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
University of Copenhagen

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Muscle mitoquinone mesylate concentration Concentration of mitoquinone mesylate in skeletal muscle Before oral administration of MitoQ
Primary Muscle mitoquinone mesylate concentration Concentration of mitoquinone mesylate in skeletal muscle 1 hours after oral administration of MitoQ
Primary Muscle mitoquinone mesylate concentration Concentration of mitoquinone mesylate in skeletal muscle 3 hours after oral administration of MitoQ
Primary Muscle mitoquinone mesylate concentration Concentration of mitoquinone mesylate in skeletal muscle 5 hours after oral administration of MitoQ
Secondary Blood mitoquinone mesylate concentration Concentration of mitoquinone mesylate in venous blood Before as well as 0.5, 1, 1.5, 2, 3, 4 and 5 hours after oral administration of MitoQ
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