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The effects of plant extract intake on male anti-fatigue and QOL

The effects of plant extract intake on male anti-fatigue and QOL - The effects of plant extract intake on male anti-fatigue and QOL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055821
Enrollment
50
Registered
2024-12-30
Start date
2024-10-30
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 Adults

Interventions

Consumption of food containing plant extracts Consumption of food placebo

Sponsors

EAS Inc.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: (1) Healthy men in their 30s to 50s who are concerned about the decline in male function in recent years (2) Those with a BMI of less than 30kg/m2 (3) Men who are not currently engaging in sexual activity with the aim of becoming pregnant (4) Those who are not undergoing infertility treatment (5) Those who are not currently smoking (those who have been abstaining from smoking for more than one year) (6) Those who can provide written consent to participate in the study voluntarily

Exclusion criteria

Exclusion criteria: (1) Those currently taking medication for any kind of disease (2) Those taking the test food or health food products containing the active ingredient of the test food (3) Those with functional erectile dysfunction (4) Those with serious diseases of the sugar metabolism, lipid metabolism, liver function, kidney function, heart, circulatory system, respiratory system, endocrine system, immune system, or nervous system, or those with mental disorders. and those with a history of such conditions (5) Those who have been judged to have a problem with participating in the trial due to abnormalities in their clinical test values in their most recent health checkup, etc. (6) Those with a current illness or a history of a serious illness that required medication (7) Those who may develop an allergy in relation to the study (8) Those who are judged to be unsuitable as test subjects based on the results of the lifestyle questionnaire (9) Those who are participating in other clinical research at the start of this study (10) Those who are judged to be unsuitable for participation in the study by the principal investigator (or the person in charge of conducting the study)

Design outcomes

Primary

MeasureTime frame
Quality of daily life, fatigue

Secondary

MeasureTime frame
Salivary testosterone

Countries

Japan

Contacts

Public ContactShigenori Nibun

EAS Inc. Clinical Trial Session

info@eas-ct.jp045-228-5243

Outcome results

None listed

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