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A safety study of test food intake in healthy adults

A safety study of test food intake in healthy adults: Open-label study - A safety study of test food intake in healthy adults: Open-label study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000061735
Enrollment
15
Registered
2026-06-10
Start date
2026-06-11
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

Sponsors

Miura Clinic, Medical Corporation Kanonkai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Subjects of men and women aged 20 to 64 (2) Subjects with a BMI of 25 or more and less than 30 (3) Subjects who received sufficient explanation about the purpose and content of the test, had the ability to consent, voluntarily volunteered to participate after understanding it well, and agreed to participate in the test in writing.

Exclusion criteria

Exclusion criteria: (1) Subjects with a history of serious diseases such as mental disorders, diabetes, liver diseases, renal diseases, gastrointestinal diseases, cardiac diseases, respiratory diseases, peripheral vascular diseases, or other serious diseases. (2) Subjects who have undergone gastrointestinal surgery. (3) Subjects with abnormal liver and renal function test values. (4) Subjects with diseases currently being treated. (5) Subjects who are allergic to food or drugs. (6) Subjects with symptoms of anemia. (7) Female subjects who wish to become pregnant during the study, or who are pregnant (including those who may be pregnant) or lactating. (8) Subjects who play intense sports or who are on a diet. (9) Subjects with extremely irregular eating habits. (10) Subjects who cannot stop taking health foods (including foods for specified health use and foods with functional claims) or quasi-drugs during the study period. (11) Subjects who are continuously treated with pharmaceuticals (including OTC and prescription drugs). (12) Subjects who drink more than 60 g of pure alcohol per day. (13) Subjects who smoke more than 21 cigarettes per day on average. (14) Subjects who are participating in or will participate in other clinical trials at the start of this study. (15) Subjects who are judged by the investigator or subinvestigator to be inappropriate for the study.

Design outcomes

Primary

MeasureTime frame
Medical interview Physical examination Laboratory test values Adverse event

Countries

Japan

Contacts

Public ContactMakoto Terashima

Oneness Support Co., Ltd. Clinical Trial Division

mterashima@oneness-sup.co.jp06-4801-8917

Outcome results

None listed

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