About this trial
Polycystic Ovary Syndrome (PCOS) is one of the most common endocrine disorders among women of reproductive age, characterized by chronic anovulation, hyperandrogenism, and polycystic ovarian morphology. Letrozole, an aromatase inhibitor, has emerged as a first-line ovulation induction agent due to its superior ovulation and pregnancy rates compared to clomiphene citrate. Estradiol valerate, a synthetic estrogen, can be co-administered with letrozole to improve endometrial receptivity by enhancing endometrial thickness, vascularity, and pattern. This study aims to evaluate the effect of letrozole alone versus letrozole with estradiol valerate on endometrial development in these patients.
Eligibility criteria
Qualifiers
Women aged 20-35 years
Clinical diagnosis of PCOS (Rotterdam criteria)
Disqualifiers
Endocrine disorders other than PCOS
Endometrial pathology or uterine malformations
Allergy to letrozole or estradiol
Hormonal therapy within last 3 months
Trial design
Treatments tested in this trial
- Letrozole (Aromatase Inhibitors)
- Letrozole (Aromatase Inhibitors) + Estradiol valerate
Treatment groups
Locations
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