Study the effects of probiotic supplementation on polycystic ovary syndrome
Phase 3
Recruiting
- Conditions
- Polycystic ovary syndome.Polycystic ovarian syndrome
- Registration Number
- IRCT20180404039187N3
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 84
Inclusion Criteria
patients whom have polycystic ovary syndrome based on the ultrasond tests
Exclusion Criteria
hypertension
Hyperprolactinemia
Renal failure
Liver failure
Heart failure
Cancer
Diabetes
Hyperthyroidism
Hypothyroidism
Smoking
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fasting blood sugar level. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(enzymatic).;Testestrone. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(immuno assay).;Dehydroepiandrosterone sulfate. Timepoint: At the beginning and 3 months later. Method of measurement: laboratory tests(immuno assay).
- Secondary Outcome Measures
Name Time Method