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Effect of supplementation in treatment of polycystic ovary syndrome

Not Applicable
Conditions
Polycystic ovary syndrome.
Sclerocystic ovary syndrome Stein-Leventhal syndrome
E28.2
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
NameTimeMethod
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
NameTimeMethod
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