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Effect of combined probiotic and vitamin D supplementation in the treatment of polycystic ovary syndrome

Phase 3
Conditions
Polycystic ovary syndrome.
Polycystic ovarian syndrome
E28.2
Registration Number
IRCT20170513033941N37
Lead Sponsor
ational Institute for Medical Research Development of Iran (NIMAD)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Patients with polycystic ovary syndrome
Individuals aged 18 to 40 years.

Exclusion Criteria

Pregnant women
Lactation
Adrenal hyperplasia
Androgen-secreting tumors
Hyperprolactinemia
Thyroid dysfunction
Diabetes
Psychological or psychiatric disorders such as anxiety or depressive symptoms at the enrollment

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total testosterone. 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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