Effects of Nigella Sativa in Obese Wome
Phase 2
- Conditions
- Obesity.Obesity due to excess calories
- Registration Number
- IRCT201106191197N10
- Lead Sponsor
- Vice Chancellor for research of Tabriz Uniersity of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 82
Inclusion Criteria
women with 25-50 years old; Body Mass Index between 30 to 34.9 kg/m2; following no weight loss diet or any special diet during 6 months ago. Exclusion criteria: taking vitamin-mineral supplement during 3 months ago;taking anti-inflammatory medications, losing weight drugs, asprin and other anticoagulant medications; cardiovascular diseases, liver, kidney and tyroid disorders,type 1 or 2 diabetes; pregnancy and lactation; smoking
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Anthropometric indices. Timepoint: Beginning and at the end of the intervention(after 2 months). Method of measurement: Height,weight,waist circumference,hip circumference mesearment.;Inflammatory factors. Timepoint: Beginning and at the end of the intervention( after 2 months). Method of measurement: Measurement of IL-6,TNF-a and hs-CRP with special kits.;Lipid profile. Timepoint: Begining and at the end of study(2 months). Method of measurement: Measurment of HDL-C,LDL-C,TG,TC with special kits.
- Secondary Outcome Measures
Name Time Method Frequency of adiponectin and PPAR gamma-2 genotypes. Timepoint: Begining of intervention. Method of measurement: PCR-RFLP.