Comparison of Two Ovarian Stimulation Protocols in Polycystic Ovarian Syndrome (PCOS) Patients Undergoing IVF/ICSI

Not Applicable

Recruiting

• Conditions: Polycystic ovarian syndrome.; Polycystic ovarian syndrome; E28.2

• Registration Number: IRCT20080831001141N33
• Lead Sponsor: Royan Institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 232

Inclusion Criteria

The major criteria for diagnosis of PCOS are oligo and/or anovulation, clinical or biochemical signs of hyperandrogenism and polycystic ovaries; these criteria are in accordance with the revised 2003 Rotterdam criteria for PCOS
Age between 18 to 39 years
Body mass Index (BMI) less than 30 kg/m2

Exclusion Criteria

Clinically significant systemic disease such as renal failure
Endometriosis grade 3 or higher
Received hormonal treatments in the previous 3 months
Any contraindications to ovarian stimulation
Sever male factor (TESE-PESA)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Fertilization rate. Timepoint: 16-18 hours after sperm insemination or injection. Method of measurement: The ratio between the number of zygotes with two pronucleus and the injected oocytes.