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Ribose and Sport Performance

L

Laval University

Status

Completed

Conditions

Sports

Treatments

Other: Ribose
Other: Placebo

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01727479
2012-048
INAF-2012-048

Details and patient eligibility

About

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

Enrollment

18 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

18 participants in 2 patient groups, including a placebo group

Ribose
Experimental group
Description:
After each of the 3km time trial (3 in total), consumption of ribose incorporated in a sports drink.
Treatment:
Other: Ribose
Placebo
Placebo Comparator group
Description:
After each of the 3km time trial (3 in total), consumption of placebo incorporated in a sports drink.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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