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Comparison Between Two Fertility Protocols in Obese Polycystic Ovary Syndrome Patients

Infertility Clinical Trial

Official title:
Comparison Between Two Fertility Protocols in Obese Polycystic Ovary Syndrome

Clinical Trial Summary

The purpose of this study is to compare two fertility protocols in obese women with Polycystic Ovarian Syndrome who are candidates for In Vitro Fertilization (IVF). These protocols carry less risk of ovarian hyperstimulation syndrome which these women may experience.

Clinical Trial Description

The purpose of this study is to compare two fertility protocols in obese women with Polycystic Ovarian Syndrome who are candidates for In Vitro Fertilization (IVF). These protocols carry less risk of ovarian hyperstimulation syndrome which these women may experience.The patients in the IVM group will not be exposeD to gonadotropin treatment for controlled ovarian hyperstimulation. In the antagonist group we will use GnRH agonist to induce ovulation which may reduce the risk for ovarian hyperstimulation. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01473459
Study type Interventional
Source Hillel Yaffe Medical Center
Contact Tal Shavit, MD
Phone 972-50-6246712
Email tal.shavit@gmail.com
Status Not yet recruiting
Phase N/A
Start date April 2012
Completion date January 2013
View Details
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