Safety-confirmation of excessive ingestion of test food
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000047547
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Not provided
(1) Subjects who take steadily in the health-specific/functional/supplementary/health foods, and will have any difficulty in giving up taking them after the consent. (2) Subjects who have taken some kind of medicine, and have any difficulty in refraining from taking them during this research. (3) Subjects with excessive alcohol intake. (4) Subjects with current and/or previous medical history of serious diseases in heart, liver, kidney and/or digestive organs. (5) Pregnant, possibly pregnant women during this research, or lactating ones. (6) Subjects with drug and/or food allergy. (7) Subjects who are now under other clinical researches with some kind of medicine/food, or participated in those within four weeks before this research, or planning to join those after the consent. (8) Subjects who donated over 200 mL of their blood and/or blood components within a month to this research. (9) Males who donated their whole blood (400 mL) within the last three months to this research. (10) Females who donated their whole blood (400 mL) within the last four months to this research. (11) Males who will be collected in total of their blood (1200 mL) within the last twelve months, after adding the blood amounts planning to be sampled in this research. (12) Females who will be collected in total of their blood (800 mL) within the last twelve months, after adding the blood amounts planning to be sampled in this research. (13) Others who have been determined as ineligible for participation in this research, according to the principal/sub investigator's opinions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method