Blood kinetics study of a single intake of the test food in healthy adult male subjects.
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000051827
- Lead Sponsor
- FANCL Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 10
Not provided
1)Subjects with a serious medical history, or with a history of disorders of the digestive system, circulatory system (e.g., heart failure), endocrine system, etc. Subjects who have been judged to be inappropriate for the study by the principal investigator. 2)Subjects who have a history of gastrointestinal resection surgery, excluding appendectomy. 3)Subjects who are currently taking medication or being treated by a physician. 4)Subjects who must be scheduled to receive medical treatment or medication during the study period. 5)Subjects who plan to consume health foods or supplements other than the food under study after consent. 6)Subjects who are unable to consume the test food due to preference or allergy. Subjects who may have allergies related to the test food. 7)Heavy drinkers of alcohol and smokers. 8)Subjects who donated blood over 200mL in the past 4 weeks or over 400mL in the past 12 weeks. 9)Subjects who currently or will be participating in another clinical research study during the study period. 10)Subjects who have irregular sleep or eating habits due to night work or insomnia. 11)Subjects who are engaged in strenuous physical activity. 12)Subjects judged as unsuitable for the study by the responsible doctor for other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood kinetics (Cmax)
- Secondary Outcome Measures
Name Time Method Blood kinetics (Blood concentration, AUC, Tmax, T1/2)