Suppressive effect of test food on postprandial serum triglyceride level
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000027893
- Lead Sponsor
- CPCC Co.,Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Not provided
(1) Subjects who use oral medication, supplements and/or functional foods affecting lipid metabolism (2) Subjects who are pregnant or breast-feeding, or have the will of pregnancy during the study period (3) Subjects who are suffered from or under treatment of serious disease (e.g., heart disease, liver disease, kidney disease, and/or digestive disease) (4) Subjects who are under treatment of alcohol dependence (5) Subjects who are extremely irregular in eating habits (6) Subjects who declare the allergy symptoms against drugs and/or foods (7) Subjects who are participating in other clinical trials of drugs or health food, who participated in the last 4 weeks, or who are willing to participate after giving the informed consent (8) Subjects who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study (9) Males who have donated over 400 mL of blood and/or blood component within the last three months prior to the current study (10) Females who have donated over 400 mL of blood and/or blood component within the last four months prior to the current study (11) Males whose total blood collection volume exceeding 1200 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (12) Females whose total blood collection volume exceeding 800 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (13) Subjects who are predicted to be difficult to comply with agreements and subject management (14) Subjects who are judged as unsuitable for the study by the investigator for the other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time course of delta AUC (area under the curve) and delta serum triglyceride level
- Secondary Outcome Measures
Name Time Method Time course of AUC (area under the curve) and serum triglyceride level