Evaluation of lipid metabolism-improving effects by taking a single dose of test beverage
- Conditions
- Healthy male adults
- Registration Number
- JPRN-UMIN000043326
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 40
Not provided
(1) Subjects with previous and/or current medical history of serious diseases in circulatory/respiratory/digestive/urinary organs. (2) Throughout this trial, subjects who have any difficulty in refraining from taking steadily in the medicines (related to blood pressure, fatigue, lipid, and/or allergic rhinitis), which might affect the test results. (3) Subjects taking steadily in the following foods that might affect their test result; health-specific, functional, health foods (related to blood pressure, blood stream, exercise fatigue, metabolism-improving, poor blood flow-improving, fat combustion and/or lipolysis), supplementary one, vitamin tablet and nutrient, with any difficulty in refraining from having those during this trial. (4) Subjects who take excessive alcohol. (5) Subjects with any possibility of hindrance to this trial, owing to their allergic rhinitis. (6) Subjects who are now under the other clinical tests with some kind of medicine/food, or participated in those tests within four weeks before this trial. (7) Subjects falling into the habit of smoking. (8) Subjects suffering from severe anemia. (9) Subjects having drug and/or food allergy. (10) Subjects who donated over 200 mL of their whole blood and/or blood components within a month before this trial. (11) Subjects who donated over 400 mL of their whole blood within the last three months before this trial. (12) Subjects who will be collected over 1200 mL of their blood within the last twelve months before this trial. (13) Others who have been determined as ineligible for participation, judging from the principal/sub investigator's opinions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method