None
Conditions
Interventions
Oral ingestion of the test food for 16 weeks
Oral ingestion of the placebo food for 16 weeks
Sponsors
KSO Corporation
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Subjects aged more than 20 years, less than 65 years 2) Subjects of BMI between 23 and 30
Exclusion criteria
Exclusion criteria: 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body composition(abdominal fat, body fat) | — |
Secondary
| Measure | Time frame |
|---|---|
| Anthropometry, Serum lipids, Blood glucose-related variables, Liver function, Inflammatory marker | — |
Countries
Japan
Contacts
Public ContactEiji Yoshikawa
KSO Corporation Sales department
Outcome results
None listed