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Comparison Between Two Fertility Protocols in Obese Polycystic Ovary Syndrome Patients

H

Hillel Yaffe Medical Center

Status

Unknown

Conditions

Obese
Infertility
Polycystic Ovary Syndrome

Treatments

Procedure: IVM (In Vitro Maturation) Treatment
Procedure: IVF (In Vitro Fertilization) Antagonist Protocol

Study type

Interventional

Funder types

Other

Identifiers

NCT01473459
0078-11-HYMC

Details and patient eligibility

About

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.

Full 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.

Enrollment

40 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • BMI > 30
  • PCOS
  • Failure of COH treatment

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

IVM Treatment
Active Comparator group
Treatment:
Procedure: IVM (In Vitro Maturation) Treatment
Antagonist Protocol
Active Comparator group
Treatment:
Procedure: IVF (In Vitro Fertilization) Antagonist Protocol

Trial contacts and locations

1

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Central trial contact

Tal Shavit, MD

Data sourced from clinicaltrials.gov

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