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A study to compare the absorbency after test food intake.

A study to compare the absorbency after test food intake. - A study to compare the absorbency after test food intake.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042720
Enrollment
24
Registered
2020-12-12
Start date
2020-12-12
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

None

Interventions

Single intake of food A and placebo-Wash out-Single intake of food B-Wash out-Single intake of food C and placebo Single intake of food B-Wash out-Single intake of food C and placebo-Wash out-Single i

Sponsors

APO PLUS STATION CO., LTD.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Japanese healthy males and females aged from 20 to 59 years old 2)Subjects who can visit the medical institution where the test is conducted on the scheduled visit date and can be hospitalized for 2 nights and 3 days in this test 3)Subjects who have an ability to understand the purpose and contents of this clinical trial and voluntarily applied and agreed to participate in this clinical trial after the explanation of this clinical trial

Exclusion criteria

Exclusion criteria: 1)Subjects who regularly use foods containing the ingredients used in this test 2)Subjects who usually intake a food for specified health use, functional food and health foods 3)Subjects who weigh 40 kg or less or 100 kg or more, or who have a BMI of 31 or more 4)Subjects who are under treatment or have a history of serious heart disease, lung disease, gastrointestinal disease, hypertension, diabetes, or malignant neoplasms 5)Subjects who usually intake drug 6)Subjects who are pregnant, lactation, or planning to become pregnant 7)Subjects who are sensitive to test product or other foods, and medical products 8)Subjects who have collected more than 200 mL of blood 4 weeks before the Screening test or 400 mL of blood before 16 weeks before the Screening test 9)Subjects who have had a bad mood or poor physical condition due to blood sampling in the past 10)Subjects who participated in other clinical studies 11)Subjects who are judged as unsuitable for this study by the principal investigator for other reasons

Design outcomes

Primary

MeasureTime frame
AUC Cmax

Secondary

MeasureTime frame
Tmax T1/2

Countries

Japan

Contacts

Public ContactFukuko Kubota

APO PLUS STATION CO., LTD. CRO Department Clinical Operations Division

food-contact@apoplus.co.jp03-6386-8809

Outcome results

None listed

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