polycystic ovary syndrome. Polycystic ovarian syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: having poly cystic ovary syndrome according to the Rotterdam criteria; age between 20-45 years; not pregnant or lactating; non adherence to specific regime during the past 3 months; no smoking; no chronic diseases including, diabetes, cardio-vascular, liver, kidney, thyroid; non-food supplements; being overweight (BMI= 25 Kg/m2) Exclusion criteria: hormone therapy; pregnancy and lactation during the study; weight loss (more than 2.5 kg per month) during the study
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Serum Insulin Level. Timepoint: Baseline, week 8. Method of measurement: Enzyme-Linked Immunosorbent Assay. | — |
Secondary
| Measure | Time frame |
|---|---|
| Insulin Resistance. Timepoint: Baseline, week 8. Method of measurement: Calculation.;Fasting Blood Sugar. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;Quantitative Insulin Sensitivity Check Index. Timepoint: Baseline, week 8. Method of measurement: Calculation.;Homeostatic Model Assessment of Insulin Resistance. Timepoint: Baseline, week 8. Method of measurement: Calculation.;Homeostatic Model Assessment of Beta-cell function. Timepoint: Baseline, week 8. Method of measurement: Calculation.;High Density Lipoprotein. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;Low Density Lipoprotein. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;Total Cholesterol. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;Androgen. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;Testosterone. Timepoint: Baseline, week 8. Method of measurement: Commercial kits.;C-Reactive Protein. Timepoint: Baseline, week 8. Method of measurement: Enzyme-Linked Immunosorbent Assay. | — |
Countries
Iran (Islamic Republic of)
Contacts
Isfahan University of Medical Sciences