A clinical study to evaluate the effects of beverage containing green tea catechins on reducing LDL cholesterol
- Conditions
- one
- Registration Number
- JPRN-UMIN000031224
- Lead Sponsor
- Soiken Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 140
Not provided
1) Subjects receiving a medical treatment for dyslipidemia 2) Subjects having serious hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders 3) Subjects whose fasting serum triglyceride levels are 400 mg/dL or more 4) Subjects who have the possibility of developing allergic symptoms by the test food 5) Subjects who take Foods for Specified Health Uses or Foods with Function Claims labeled the effects of improving LDL cholesterol or total cholesterol levels 6) Subjects who take foods having the effects of improving LDL cholesterol or total cholesterol levels 7) Female subjects who are pregnant or lactating, or intending to be pregnant during the study 8) Female subjects who have menstrual irregularities 9) Subjects who have extremely irregular dietary habits, work in shifts or work during the night 10) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 11) Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 12) Subjects deemed unsuitable by the investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method