Healthy adults
Conditions
Interventions
Single ingestion of test food B >
Single ingestion of test food A (5mg) >
Single ingestion of test food A (20mg) >
Single ingestion of test food A (80mg)
Sponsors
SOUSEIKAI Fukuoka Mirai Hospital
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1) Subjects who are voluntarily giving written informed consent. 2) Healthy males aged between 20 and 60. 3) Subjects who can take meals, eat test foods, take blood samples, take urine samples and stay quiet and rest on the schedule indicated by investigators.
Exclusion criteria
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.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Plasma metabolites concentration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Urinary metabolites concentration. | — |
Countries
Japan
Contacts
Public ContactJunko Manabe
SOUSEIKAI Fukuoka Mirai Hospital Clinical Research Center, Planning and Coordination Dept.
Outcome results
None listed