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The effect of oral amino acids on physical function

The effect of oral amino acids on physical function - The effect of oral amino acids on physical function

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000021525
Enrollment
24
Registered
2016-03-31
Start date
2016-04-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy volunteers

Interventions

Intake of placebo for 7 days -&gt
washout period for more than 3 weeks -&gt
intake of amino acids for 7 days Intake of amino acids for 7 days -&gt
intake of placebo for 7 days

Sponsors

Juntendo University, Graduate School of Health & Sports Science
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Male collegiate soccer players PWC75%HRmax is more than 160W Subjects who have a briefing of the content of the present study, fully understanding and agreeing to its objective and being able to personally sign a written informed consent Subjects who can pedal ergometer at more than 60 rpm for 12min on work rate of 60rpm and PWC75%HRmax.

Exclusion criteria

Exclusion criteria: 1) Subject having medical treatment in a hospital or clinic 2) Subject having treatment or previous history for serious cardiovascular, respiratory, endocrine, or metabolic disorders 3) smoker 4) Subject who ended participation in another clinical trial less than 3 months before 5) Subject having cedar or cypress pollen allergy 6) Subject who has had a blood sample of 200 ml or more taken (e.g., donated blood) within 1 month, or 400 ml or more within 3 months of the start of the present study 7) Subjects who have an intake of amino acids supplement 8) Subject deemed unsuitable by the investigator 9) Subject having previous history for chest pain or faint 10) Subjects who have participated in other clinical study within the last 3 months prior to the current study or are participating in other clinical study currently

Design outcomes

Primary

MeasureTime frame
Ergometer (1week after administration)

Secondary

MeasureTime frame
Psychological tests by using the visual analog scale (VAS) blood examination

Countries

Japan

Contacts

Public ContactYoshio Suzuki

Juntendo University Graduate School of Health and Sports Science

yssuzuki@juntendo.ac.jp0476-98-1001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026