Over weight(BMI>
Conditions
Interventions
The subjects take the test food during 3 months.
The subjects take the placebo food during 3 months.
Sponsors
Kyoto Prefectural University Of Medicine
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1)30yrs<=age<=65yrs 2)Male 3)Outpatients 4)BMI>=25 5)Those who are able to take the test foods during 3 months. 6)Those who don't change the diet or exercise regimen during the study period 7)consent document
Exclusion criteria
Exclusion criteria: 1)People corresponding to the following *LDL-Cholesterol>=180mg/dl *Systolic blood pressure>=160mmHg *Diastolic blood pressure>=90mmHg *Hemoglobin A1c>=6.5% *Fasting blood glucose>=140mg/dl 2)Smokers 3)People of dyslipidemia treatment during administration 4)serious heart disease(heart failure,myocardial infarction,myocarditis,etc.)liver disease(liver failure symptoms (fulminant hepatitis),patients with cirrhosis of the liver,liver tumor),renal disease(nephrotic syndrome,renal failure (acute and chronic), uremia, merged, etc.hydronephrosis) 5)Patients who took antihypertensive drugs 6)Those who have participated in other clinical trials within before consent get one month,and those who are currently participating in other clinical trials. 7)At the physician's judgment,who it is determined that there is a possibility that either increased risk to the subject,or sufficient data not obtained
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visceral fat area | — |
Countries
Japan
Contacts
Public ContactYoshitada Hira
IMEQRD Co., Ltd. Planning and Sales Department
Outcome results
None listed