Status:

COMPLETED

Setria Performance Blend Supplementation

Lead Sponsor:

University of North Carolina, Chapel Hill

Collaborating Sponsors:

Kirin Holdings Company, Limited

Conditions:

Healthy

Eligibility:

MALE

20-30 years

Phase:

NA

Brief Summary

The objective of this trial is to evaluate the effects of setria performance blend supplementation on endurance performance in healthy men.

Detailed Description

This study is a randomized, double-blind, placebo-controlled crossover trial in healthy men. Subjects will take either a placebo or setria performance blend (L-citrulline + glutathione) for 8 days. At...

Eligibility Criteria

Inclusion

  • Participant is an adult male between the ages of 20-30 years
  • Participant is aerobically fit, as defined by a VO2max between 42-70 ml\*kg/min (determined by the screening test)
  • Participant is not obese (18.5 ≦ BMI \< 30 kg/m²)
  • Participant has provided written and dated informed consent to participate in the study
  • Participant is willing and able to comply with the protocol
  • Participant is apparently healthy and free from disease, as determined by a health history questionnaire
  • Participant agrees to refrain from strenuous exercise and alcohol consumption within 24 hours of laboratory visits, and to refrain from caffeine consumption within twelve hours of visits
  • Participant agrees to refrain from using antibacterial mouthwash, chewing gum, and brushing their teeth on the morning of laboratory visits

Exclusion

  • Participant has consistently used prescription drugs or ergogenic dietary supplements that may influence study outcomes within eight weeks prior to enrollment, or begins to do so during the study. Potential drugs and supplements include but are not limited to whey protein, creatine, beta-alanine, antihypertensive medications, or anabolic steroids
  • Participant has gained or lost ≥10 lbs in the previous 2 months
  • Participant is enrolled in a separate clinical trial involving diet, exercise, physical activity, or the potential ingestion of an active drug or dietary supplement in the previous 2 months and during this study
  • Participant has participated in a clinical trial within the previous 2 months that includes modifications to their physical and/or diet that may influence study outcomes and during this study
  • Participant has a known allergy or sensitivity to the placebo or active ingredients
  • Participant consumes more than 3 alcoholic drinks per day
  • Participant has used tobacco more than three days per week (on average) in the previous eight weeks
  • Participant has used recreational drugs within the past month, or refuses to abstain from recreational drug use for the entirety of the study

Key Trial Info

Start Date :

November 30 2019

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

November 1 2020

Estimated Enrollment :

25 Patients enrolled

Trial Details

Trial ID

NCT04090138

Start Date

November 30 2019

End Date

November 1 2020

Last Update

April 20 2021

Active Locations (1)

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Applied Physiology Laboratory, Fetzer Hall Room 25

Chapel Hill, North Carolina, United States, 27599