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Effect of supplementation in treatment of women with polycystic ovary syndrome

Phase 3
Conditions
Polycystic ovary syndrome.
Polycystic ovary syndrome
E28.2
Registration Number
IRCT201701165623N103
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
60
Inclusion Criteria

Patients with PCOS according to Rotterdam criteria
Aged 18 to 40 years

Exclusion Criteria

Intake of magnesium, zinc, calcium and/or vitamin D supplementswithin the past 3 months.
Pregnant women
Metabolic disorders, including hyperandrogenism, Cushing’s syndrome, androgen secreting tumors, hyperprolactinemia.
Thyroid dysfunction
Not residing in Arak area

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Insulin. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Elisa kit.;Insulin resistance. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Calculation using HOMA formula.;Fasting plasma glucose. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Enzymatic kit.;Total testosterone. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Elisa kit.;SHBG. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: Elisa kit.
Secondary Outcome Measures
NameTimeMethod
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