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A study for the effect of the intake of ONO-SR/AST on male vitality

A study for the effect of the intake of ONO-SR/AST on male vitality - A study for the effect of the intake of ONO-SR/AST on male vitality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000040728
Enrollment
110
Registered
2021-10-24
Start date
2020-06-15
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 adult

Interventions

Sponsors

TTC Co., Ltd
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Males from 35 to 65 years of age

Exclusion criteria

Exclusion criteria: (1) Subjects who constantly use health food richly containing involvement ingredient (2) Subjects at risk of developing allergy in relation to the study. (3) Subjects taking drugs that may affect the results of the study (4) Subjects having a history of serious diseases for which medication was required (5) Subjects having a drug dependence, alcohol dependence requiring treatment or a history of serious alcohol dependence (6) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on the pre-treatment test. (7) Subjects who donated or transfused 200 mL or 400 mL of whole blood within 3 months before the pre-treatment test. (8) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study. (9) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (10) Subjects who cannot protect contraception during the study period (11) Subjects judged as unsuitable for the study by the investigator for other reasons

Design outcomes

Primary

MeasureTime frame
Tests for male vitality

Countries

Japan

Contacts

Public ContactChiharu Goto

TTC Co., Ltd. Clinical Research Planning Department

c.goto@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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