A study to evaluate the efficacy of D-Ppsicose on weight reduction in overweight subjects
- Conditions
- Endocrine, nutritional and metabolic disease
- Registration Number
- KCT0002081
- Lead Sponsor
- The Catholic University of Korea
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 99
99 overweight or obese patients (body mass index [BMI] between 23 kg/m2 and 30 kg/m2 ) aged between 19 and 65 years
- For women of childbearing age , negative pregnancy test during screening
- individuals agreed to participate in the study voluntarily after sufficient explanation regarding the purpose and content of study
The exclusion criteria included (1) Current or past history of any malignant diseases during the past 5 years ; (2) hypersensitivity to D-psicose; (3) Current psychiatric illness or psychotropic medication; (4) History of participation in any weight loss program 3 months before screening; (5) Pregnancy or breast feeding; (6) weight stable (±5%) for 3 months prior to their study participation; 7) Current use of drug that can affect the weight (weight-loss drugs, Dietary Supplements, oral corticosteroid, thyroid hormon, cyproheptadine, phenothiazine, oral contraceptive; (8) abnormal renal function or hepatic function test: and (9) The presence of diabetes or unstable cardiovascular disease.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method body fat mass change
- Secondary Outcome Measures
Name Time Method visceral and liver fat assessed by CT;Waist circumference;body mass index (BMI, kg/m2) and body weight;cardiovascular risk factors: fasting lipid concentrations (total cholesterol, highdensity lipoprotein [HDL] cholesterol, low-density lipoprotein [LDL] cholesterol, and triglycerides [TG]), glucose, insulin, and C-reactive protein;adverse events and safety