Effect of supplementation in treatment of polycystic ovary syndrome
Not Applicable
- Conditions
- Polycystic ovary syndrome.Sclerocystic ovary syndrome Stein-Leventhal syndromeE28.2
- Registration Number
- IRCT201306085623N8
- Lead Sponsor
- Vice chancellor for research, Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 81
Inclusion Criteria
Women aged 18-40 years diagnosed with PCOS
Exclusion Criteria
Women aged<18 or >40 years
Those with BMI<25 kg/m2, individuals with neoplastic, hepatic, renal and cardiovascular disorders
Malabsorptive disorders
Current or previous (within the last 6 months) use of hormonal
Antidiabetic medications
Anti-obesity medications
Intention to adopt a diet and/or a specific physical activity program
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Insulin. Timepoint: At the beginning of the study and after 8 weeks of intervention. Method of measurement: Elisa.;Hs-CRP. Timepoint: At the beginning of the study and after 8 weeks of intervention. Method of measurement: Elisa.
- Secondary Outcome Measures
Name Time Method