The clinical trial of blood kinetics upon the ingestion of fat-soluble foods.
- Conditions
- one(Healthy subjects)
- Registration Number
- JPRN-UMIN000039504
- Lead Sponsor
- Medical Corporation Hokubukai Utsukushigaoka Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 30
Not provided
(1) Subjects with hepatic, renal, cardiac or organ disorders or diabetes or other serious diseases. (2) Subjects with a surgical history of the digestive system (except appendicectomy). (3) Subjects with a history of a drug or food allergy. (4) Subjects currently under treatment with chronic diseases. (5) Subjects who are pregnant or intend to become pregnant during the study or are lactating. (6) Subjects who cannot restrict the intake of foods that may influence the measurement of the samples during the study. (7) Subjects who take excessive alcohol (equivalent to 60 g pure ethanol/day in average consumption). (8) Subjects who participate in other clinical trials. (9) Subjects who have a history of feeling ill or unwell during or after the blood draw. (10) Subjects who have donated over 400 mL of blood within the last three months prior to the screening of this study or expect to donate the same during the study. (11) Subjects with extremely irregular diet (night-shift worker, etc). (12) Subjects who have smoked within 6 months. (13) Subjects who need to avoid taking the foods that do not clearly indicate the origin of all ingredients, because of religions, etc. (14) Subjects judged as unsuitable for this study by the investigator for other reasons.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method