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Assesment the clinical effect of myoinositol on insulin resistence in women with PCOS

Phase 2
Conditions
Polycystic Ovarian Syndrome.
Ovarian dysfunction, unspecified
Registration Number
IRCT2015010319426N4
Lead Sponsor
Vice chancellor for research, Shahid Beheshti University of Medical Science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
50
Inclusion Criteria

women who were between 20 and 40 years old, and had PCOS diagnosed by a gynecologist.
Exclusion criteria: patients who were diagnosed with Cushing syndrome, congenital adrenal hyperplasia, hyperprolactinemia, hypothyroidism, hyperthyroidism, androgen secreting tumor; medications known to affect metabolic parameters, such as metformin and corticosteroids.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fasting glucose. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;Fasting insulin. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;HOMA IR. Timepoint: Before intervention and three months after treatment. Method of measurement: Calculation by formola.
Secondary Outcome Measures
NameTimeMethod
Weight. Timepoint: Before intervention and three months after treatment. Method of measurement: Balance.;Height. Timepoint: Before intervention and three months after treatment. Method of measurement: Meter.;Body Mass Index. Timepoint: Before intervention and three months after treatment. Method of measurement: Formola.;Low density lipoprotein. Timepoint: Before intervention and three months after treatment. Method of measurement: Blood serum.;High density lipoprotein. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Free testosterone. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Dehydoepiandrasteione. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.;Triglyceride. Timepoint: Before intervention and two months after vitamin D injection. Method of measurement: Blood serum.
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