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Effect of Yoghurt Fortified with Probiotics and Vitamins D and E in Treatment of Polycystic Ovary Syndrome

Phase 3
Recruiting
Conditions
Polycystic ovary syndrome.
Polycystic ovarian syndrome
E28.2
Registration Number
IRCT20231210060323N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
90
Inclusion Criteria

Willingness to cooperate in the study and provide written consent
Being in the reproductive age range of 18-45 years
Diagnosis of polycystic ovary syndrome based on the Rotterdam criteria
No intake of alcohol or drugs
Not pregnant or breastfeeding
No menopause
No participate in other research studies

Exclusion Criteria

Using drugs affecting blood pressure, blood lipids, ovarian function, insulin sensitivity (including metformin, incretin, and Thiazolidinediones) and oral contraceptives (including progesterone and estrogen) since 3 months before entering the study.
Taking any nutritional supplements for 3 months before entering the study
Taking drugs affecting vitamin D metabolism
having diabetes, thyroid disease or any systemic disease (such as kidney, liver, digestive system, cardiovascular system)
Having disorders that lead to an increase in androgens in the blood (such as Cushing's syndrome, hyperprolactinemia)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Homeostasis model assessment of insulin resistance. Timepoint: At the beginning of the study (before the start of the intervention) and at the end of the study (8 weeks after the start of the intervention). Method of measurement: Formula.
Secondary Outcome Measures
NameTimeMethod
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