Effect of daily ingestion of the test drink on HDL-cholesterol level: A Randomized, Placebo-Controlled, Double-Blind, Parallel Group Comparison Study
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000044228
- Lead Sponsor
- everage Brain Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 270
Not provided
1. Subjects who are under physician's advice, treatment, and/or medication for dyslipidemia and/or diabetes. 2. Subjects with familial hypercholesterolemia. 3. Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal diseases, and/or affected with infectious diseases requiring reports to the authorities. 4. Subjects with major surgical history relevant to the digestive system such as gastrectomy, gastrorrhaphy, enterectomy, etc. 5. Subjects who have had allergic reactions to drugs or foods especially based on test food, Japanese cedar, Japanese cypress, or grass. 6. Subjects who regularly use medicines, health foods, and supplements. 7. Subjects who regularly take foods containing ingredients of test food. 8. Heavy smokers. 9. Alcohol addicts. 10. Subjects with disordered lifestyle. 11. Subjects with anemia. 12. Pre- or post-menopausal women complaining of obvious physical changes. 13. Pregnant or lactating women, women who expect to be pregnant during this study or may be pregnant. 14. Subjects who currently participate in other clinical trials or participated within the last 4 weeks prior to the current study. 15. Subjects who regularly exercise. 16. Any other medical and/or health reasons unfavorable to participation in the current study, as judged by the principal investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method