Randomized, Placebo-controlled, Clinical Study to Investigate the Anti-Metabolic Syndrome Effect of the Functional Food in humans
Not Applicable
- Conditions
- Obesity
- Registration Number
- JPRN-UMIN000019041
- Lead Sponsor
- ot-for profit Organization Japan Clinical Research Support Unit
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
Not provided
Exclusion Criteria
1) Pregnancy, nursing or planning to become pregnant during the study (female only) 2) Any other significant medical conditions 3) Uncontrolled metabolic syndrome, or diabetes with insulin treatment 4) Severe allergies to wheat, soy, egg, milk, crustacean shellfish 5) Severe sensitivity to caffeine 6) Implantable electronic medical devices 7) Wearable electronic medical devices 8) Mechanical life support equipment 9) Metals as implantable materials 10) Dialysis patients 11) Participation in other clinical trials at enrollment 12) Any other considered by a study physician to be inappropriate for inclusion
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visceral fat area The start of the test after 6 weeks, 12 weeks after the start of the test
- Secondary Outcome Measures
Name Time Method