None listed
Conditions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Males equal to or more than 20 years and less than 65 years 2)Subjects with BMI >=25 kg/m2 and <30 kg/m2 3)Subjects who visit on schedule days 4)Subjects who recognize the object and contents of the study and submit the written informed consent
Exclusion criteria
Exclusion criteria: 1)Subjects who have a history of severe illness and current medical history in the heart, liver, kidney, digestive organs 2)Subjects who dyslipidemia, high blood pressure, diabetes 3)Subjects who use drugs affecting lipid metabolism, blood pressure or carbohydrate metabolism 4)Subjects who received medication treatment or surgery due to serious illness or injury within 1 month from the start of this study 5)Subjects who regularly use drugs, health foods, and supplements affecting the study 6)Heavy dinker 7)Subjects who feel bad mood by blood collection in past 8)Subjects who donated 200 mL or more of blood within 1 month from the start of the study or subjects who plan to do so during the study period 9)Subjects who have been constipated for more than 5 days 10)Shift worker 11)Subjects who plan business trip or trip for 10 days or more a month 12)Subjects who have allergy related to the study foods 13)Subjects already participating in other clinical trials 14)Subjects who are ineligible due to physician's judgment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visceral fat area | — |
Secondary
| Measure | Time frame |
|---|---|
| Subcutaneous fat area, total fat area, Body weight, BMI, Body fat percentage, Waist circumference, blood pressures (systolic and diastolic),AST(GOT),ALT(GPT),gamma-GT, total cholesterol, HDL- cholesterol, LDL- cholesterol triglyceride, glucose,sample size estimation | — |
Countries
Japan
Contacts
New drug research center, Inc. Clinical Research Dept.