Visceral fat reduction effect verification test by ingestion of plant extracts -Placebo-controlled, randomized, double-blind, parallel-group comparison study
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000053668
- Lead Sponsor
- KSO Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 90
Not provided
(1) Subjects who take medicines regularly (2) Subjects who have a current history of serious liver disease, kidney disease, gastrointestinal disease, heart disease, respiratory disease, endocrine disease, thyroid disease, adrenal gland disease, or other metabolic disease (excluding transient treatment such as colds) (3) Subjects who have a digestive disease that affects digestion and absorption, or a history of surgery (excluding appendicitis) (4) Subjects who have a history or current medical history of drug dependence or alcoholism (5) Subjects who have been diagnosed with familial hyperlipidemia (6) Subjects who are diagnosed with chronic constipation (7) Subjects who are unable to stop taking health foods and supplements (including foods for specified health uses and foods with functional claims) that may affect this study (8) Subjects who have a habit of drinking excessively (drinking more than 20 g of pure alcohol equivalent per day, at least 4 days a week) (9) Subjects who have a habit of smoking excessively (smokers of 21 cigarettes or more per day) (10) Subjects who are wearing a medical device necessary for life support, such as a cardiac pacemaker, implantable cardioverter defibrillator, or biological information monitor (11) Subjects who have a contagious disease or an injury to the palms or the soles of the feet (12) Subjects who have metal in the CT scan measurement site due to surgery, etc. (13) Subjects who are claustrophobic (14) Subjects who have reported that they are allergic to the ingredient in test foods (15) Subjects who have extremely irregular eating habits, shift workers (excluding daytime shift work), or late-night workers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The measured value of abdominal visceral fat area at 12 weeks after ingestion
- Secondary Outcome Measures
Name Time Method