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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01727479
Other study ID # 2012-048
Secondary ID INAF-2012-048
Status Completed
Phase N/A
First received November 2, 2012
Last updated December 2, 2016
Start date August 2012
Est. completion date January 2013

Study information

Verified date December 2016
Source Laval University
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Interventional

Clinical Trial Summary

Investigate the acute effect of ribose supplementation on performance and recovery in athletes.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date January 2013
Est. primary completion date January 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Men and women

- Training volume > 7hrs/week

- VO2 max > 40 and 45 mg/kg/min (for women and men respectively)

- Otherwise healthy individuals

Exclusion Criteria:

- Pregnant or breastfeeding women

- Individuals with endocrine disorders, hypercholesterolemia, cardiovascular diseases, gut diseases, cancer, anemia, hypoglycemia

- Medication for lipids, diabetes, hypertension, inflammation, autoimmune diseases, mood disorders

- Excessive alcohol consumption (more than two drinks by day for men, one for women), smoking, drug use, supplements or natural products consumption during the study

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Ribose
After each of the 3km time trial (3 in total), participants will be asked to drink the experimental product (or placebo) incorporated in a sports drink.
Placebo


Locations

Country Name City State
Canada Université Laval Québec Quebec

Sponsors (2)

Lead Sponsor Collaborator
Laval University Atrium Innovations

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Other Fatigue perception after each of the 3 consecutive 3km time trials on bike Post-exercise fatigue perception on visual analog scale (VAS) baseline and 1 week No
Other Peak Vo2 consumption during each of the 3km time trials on bike baseline and 1 week No
Primary Change in time to complete the third of 3 consecutive 3km time trials on bike baseline and 1 week No
Secondary Performance on the 3 consecutive 3km time trials on bike Performance measures: peak power (watts/kg), mean power (watts/kg), time to peak power (sec), total work (kJ) and maximum cadence (RPMmax) baseline and 1 week No
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