The three methods of ovulation induction in patients with polycystic ovarian syndrome

Not Applicable

Recruiting

• Conditions: Polycystic ovarian syndrome.; Female infertility, unspecified; N97.9

• Registration Number: IRCT20080831001141N31
• Lead Sponsor: ROYAN Institute

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 5 January 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 360

Inclusion Criteria

Infertile women with polycystic ovarian syndrome based on Rotterdam criteria
Age 20-37 years
Body Mass Index less than 30 Kg/m2
Total Motile Sperm Counts more than one million and normal morphology more than 4% (Husband)

Exclusion Criteria

Women with hematologic and autoimmune disorders
Couples with chromosomal and genetic abnormalities
Women with uterine anomalies
Women with uterine and ovaries surgical history
Women with endometriosis and adenomyosis
Women with hydrosalpinx
Women with uterine fibroids
Women with recurrent abortion history

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ive birth rate; live birth is defined in which a live fetus is delivered beyond 20 completed weeks of gestational. Timepoint: Only once; at least 20 weeks after embryo transfer. Method of measurement: Clinical information.