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Effects of PRJ-205 on Performance in Trained Young Subjects

B

Bioiberica

Status

Completed

Conditions

Healthy

Treatments

Other: Placebo
Dietary Supplement: PRJ-205

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02726516
PRJ-205

Details and patient eligibility

About

Compare a dietary supplement (PRJ-205) and placebo during 1 or 4 days on aerobic exercise performance, oxidative stress and muscle damage.

The hypothesis is that supplementation with PRJ-205 improve aerobic performance

Full description

Twenty young active males will be recruited and randomized to either placebo or PRJ-205. Subjects will take the designated treatment in an acute dosage and chronically, 4 days of treatment.

They will undergo 3 exercise tasks (before the administration of the product, 1.5h after the acute administration of the product and after 4 days of treatment). VO2max and anaerobic threshold will be measured during the tests. Blood samples will be taken to measure muscle damage and oxidative stress.

Enrollment

20 patients

Sex

Male

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Male
  • Healthy
  • Physically active

Exclusion criteria

  • known cardiovascular, pulmonary or metabolic disease
  • any medical condition that could affect the development and safety of the exercise task

Trial design

20 participants in 2 patient groups, including a placebo group

Treated
Experimental group
Description:
Treated volunteers will be administered one dose of PRJ-205 1,5 hours before the exercise task for the acute testing and will be taking one dose per day of PRJ-205 for 4 days for the chronic testing.
Treatment:
Dietary Supplement: PRJ-205
Placebo
Placebo Comparator group
Description:
Placebo volunteers will be administered one dose of placebo 1,5 hours before the exercise task for the acute testing and will be taking one dose per day of placebo for 4 days for the chronic testing.
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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