Randomized, double-blind, placebo-controlled parallel-group comparative study to evaluate the efficacy of probiotics on reducing body fat
- Conditions
- one
- Registration Number
- JPRN-UMIN000047852
- Lead Sponsor
- KSO Corporation
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Not provided
1) Subjects who have history of serious disease 2) Subjects who regularly undertake medications that affect obesity, hyperlipidemia or lipid metabolism 3) Subjects who cannot stop taking health foods or supplements that affect obesity, hyperlipidemia or lipid metabolism 4) Heavy smokers 5) Subjects who have excessive alcoholic drinks 6) Subjects with serious medication allergy or food allergy 7) Subjects who have metal in the CT scan measurement site due to surgery, etc. 8) Subjects with cardiac pacemakers or implantable cardioverter defibrillators. 9) Subject who is pregnant or under lactation, or who is expected to be pregnant during the study 10) Subjects who are currently participating, or intend to participate during this study period, in other trials involving the testing of other foods or the use of drugs or the application of cosmetics and drugs 11) Subjects who are considered to be inappropriate for this study 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