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In-Vitro Maturation of Oocytes From Polycystic Ovarian Patients Undergoing IVF


N/A
20 Years
35 Years
Not Enrolling
Female
Polycystic Ovarian Syndrome

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Trial Information

In-Vitro Maturation of Oocytes From Polycystic Ovarian Patients Undergoing IVF


Inclusion Criteria:



- Healthy women diagnosed with Polycystic Ovarian Syndrome with BMI 18-30 kg/sqm, aged
20-35

Exclusion Criteria:

- Every one else

Type of Study:

Interventional

Study Design:

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Maturation rate of oocytes, their fertilization rate, cleavage rate and embryo quality.

Outcome Time Frame:

one year

Principal Investigator

Adrian Ellenbogen, MD

Investigator Role:

Study Director

Investigator Affiliation:

IVF Unit, Hillel Yaffe Medical Center

Authority:

Israel: Israeli Health Ministry Pharmaceutical Administration

Study ID:

30/2007

NCT ID:

NCT00561808

Start Date:

January 2008

Completion Date:

January 2009

Related Keywords:

  • Polycystic Ovarian Syndrome
  • PCO/PCOD
  • IVM
  • Immature Oocytes
  • Polycystic Ovary Syndrome

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