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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000051827

Enrollment

Registered

2023-08-04

Start date

2023-08-08

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Intake of the test food.

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 1) Age, Sex: 20-34, healthy male 2) BMI: 18.5 kg/m2-24.9 kg/m2 3) Subjects who can participate in dietary interventions, intake of the test foods, blood samplings, urine samplings, and maintain rest as scheduled. 4) Subjects who voluntarily give written informed consent.

Exclusion criteria

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.

Design outcomes

Primary

Measure	Time frame
Blood kinetics (Cmax)	—

Secondary

Measure	Time frame
Blood kinetics (Blood concentration, AUC, Tmax, T1/2)	—

Countries

Japan

Contacts

Public ContactNaoyuki Abe

Medical Corporation Jikokai Shiroishi Internal Medicine Clinic Clinical Trial Division

n-abe@medi-ate.jp011-868-2711

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026