Dose-dependent anti-obesity effect of the plant extract in subjects with abdominal obesity
Not Applicable
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-UMIN000020188
- Lead Sponsor
- Hiroshima University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1) Smoker 2) Heavy user of alcohol (more than two drinks a day) 3) Taking medicines or receiving health guidance for hypertension, diabetes, and/or hyperlipidemia 4) Taking drugs or functional food that may affect the trial 5) Participation in any clinical trial within 90 days of the commencement of the trial 6) In pregnancy or nursing a child 7) Cardiac, renal, and/or hepatic dysfunction 8) History of severe disease and/or major surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visceral fat area at baseline, 8 and 12 weeks.
- Secondary Outcome Measures
Name Time Method Body weight, body fat percentage, and waist circumference at baseline, 8 and 12 weeks.