Endometrial Response in Polycystic Ovarian Syndrome Treated With Letrozole Alone or With Added Estradiol Valerate

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age20-35
SponsorCMH Kharian Medical College

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

60 Participants
are divided into 2 treatment groups

Locations

1
CMH Kharian Medical College50070, KhārianPunjab Province, Pakistan

Sponsors and collaborators

CMH Kharian Medical College

Lead sponsor