Pharmacokinetics of test food in healthy volunteers

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000041582
• Lead Sponsor: SOUSEIKAI Fukuoka Mirai Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2020-10-20
• Study Start: 2021-10-13
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: Male
• Target Recruitment: 15

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects whose clinical inspection results are outside of the normal range and who are estimated inappropriate to this study by principal investigator. 2) Subjects who have or had disorder in digestive, circulatory or endocrine system and who are estimated inappropriate to this study by principal investigator. 3) Subjects who take medicines for treatment of diseases. 4) Subjects who have food allergy. 5) Subjects who make a blood donation of 200 ml within 4 weeks before the start of the intake or that of 400 ml within 12 weeks before the start of the intake. 6) Subjects who are estimated inappropriate to participate to this study by principal investigator.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Plasma metabolites concentration.

Secondary Outcome Measures

Name	Time	Method
rinary metabolites concentration.