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Effect of Amino Acid on Muscle Damage

U

University of Toronto

Status

Completed

Conditions

Healthy

Treatments

Dietary Supplement: Active
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

The primary objective is to determine the impact of essential amino acids on integrated muscle protein synthesis over 4 days after resistance exercise.

In addition, the secondary objective is to determine the effect of essential amino acids on satellite cell regulation and inflammatory responses during this prolonged recovery period.

Enrollment

20 patients

Sex

Male

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy, male, recreationally-active participants
  • Healthy will be defined as screened by the PAR-Q+ (The Physical Activity Readiness Questionnaire for everyone; Appendix. B). Active will be defined as being in the top 20% of age specific scores on iPAQ (the International Physical Activity Questionnaire; Appendix.C).
  • Participants are required not to engage in lower limb RT (resistance training) for at least 6 months prior to the study.
  • Participants will be 18-35 years old.
  • Participants are willing to abide by the compliance rules of this study

Exclusion criteria

  • Female
  • Inability to adhere to any of the compliance rules judged by principle investigator or medical doctor
  • Self-reported regular tobacco use
  • Self-reported illicit drug use (e.g. growth hormone, testosterone, etc.)
  • The individual who has allergy for milk

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

20 participants in 2 patient groups, including a placebo group

Placebo
Placebo Comparator group
Description:
4g of maltodextrin
Treatment:
Dietary Supplement: Placebo
Active
Active Comparator group
Description:
4g of essential amino acids
Treatment:
Dietary Supplement: Active

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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