Bioavailability and Impact of Coenzyme Q10 in Stressing Exercise in Senescence Athletes
NCT03893864 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 22
Last updated 2019-03-28
Summary
It is proposed to establish a group of subjects composed of 10 healthy individuals of\> 50 years and \<65, physically active, without metabolic or inflammatory pathology. All of them will undergo a health examination and the physical condition and the absence of contraindication of the sports practice will be characterized through a monitored effort test. Each subject will take a capsule of coenzyme Q10® INDENA for 30 days. The dose to be administered is 100 mg/d of CoQ10 a with food (noon). The state of physical condition and the biochemical and biological variables that reflect oxidative stress and mitochondrial functioning before and after the intervention will be measured.
Conditions
- Coenzyme Q10
- Oxidative Stress
- Aging
Interventions
- DIETARY_SUPPLEMENT
-
Administration of a product with Fitosomed Ubiquinone
Healthy runner athletes, \> 50 years old, without any chronic illness, without any other nutritional supplementation or drug intervention, took 100 mg/d of fitosomed Ubiquinone with lunch, daily, during one month, maintaining their usual training sessions.
- PROCEDURE
-
Coenzyme Q10 level in muscle biopsies
Determination of the muscle Ubiquinone concentration, the metabolic and structure characteristics of the muscle before and after one month of supplementation
- DIAGNOSTIC_TEST
-
Coenzyme Q10 level in plasma, blood cells, urine cells
Determination of Ubiquinone concentration in different tissues before and after one month of supplementation or not
- DIAGNOSTIC_TEST
-
Total antioxidant capacity after strenous exercise
Determination of the Total Antioxidant Capacity after strenous exercise in the Climate Chamber
Sponsors & Collaborators
-
Hospital Sant Joan de Deu
collaborator OTHER -
University of Barcelona
collaborator OTHER -
Indena S.p.A
collaborator INDUSTRY -
Centre d'Alt Rendiment
lead OTHER
Principal Investigators
-
Rafael Artuch, MD, PhD · Hospital Sant Joan de Deu, Barcelona
Study Design
- Allocation
- RANDOMIZED
- Purpose
- BASIC_SCIENCE
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-03-01
- Primary Completion
- 2018-05-30
- Completion
- 2019-02-28
Countries
- Spain
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