Skip to main content
Clinical Trials/JPRN-UMIN000051827
JPRN-UMIN000051827
Completed
未知

Blood kinetics study of a single intake of the test food in healthy adult male subjects. - Blood kinetics study of a single intake of the test food in healthy adult male subjects.

FANCL Corporation0 sites10 target enrollmentAugust 4, 2023
ConditionsHealthy adults

Overview

Phase
未知
Intervention
Not specified
Conditions
Healthy adults
Sponsor
FANCL Corporation
Enrollment
10
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 4, 2023
End Date
September 30, 2023
Last Updated
last year
Study Type
Interventional
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 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.

Outcomes

Primary Outcomes

Not specified

Similar Trials