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Oocyte Cryopreservation in Assisted Reproduction


N/A
18 Years
35 Years
Not Enrolling
Female
Infertility, Egg Freezing

Thank you

Trial Information

Oocyte Cryopreservation in Assisted Reproduction


Inclusion Criteria:



1. 10 women between the ages of 18-35 inclusive at time of signing Informed Consent
Form.

2. In good general health off of current medications which may confound response to
study medications.

3. Desire to seek pregnancy actively during the study period by IVF-ICSI.

4. A normal uterine cavity must have been confirmed by either hydrosonogram or
hysteroscopy within two years of entering the study.

5. Ability to use the required medications.

6. Day 3 FSH level < 12 IU/ml

Exclusion Criteria:

1. Current pregnancy

2. Patients with significant anemia (Hemoglobin < 10 mg/dL).

3. Patients enrolled simultaneously into other investigative studies that would
interfere with this research study.

Type of Study:

Interventional

Study Design:

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Incidence of Biochemical Pregnancy

Principal Investigator

Peter G. McGovern, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

UMDNJ-NJMS

Authority:

United States: Institutional Review Board

Study ID:

IRB 0120080226

NCT ID:

NCT00839839

Start Date:

February 2009

Completion Date:

February 2011

Related Keywords:

  • Infertility
  • Egg Freezing
  • infertility
  • egg freezing
  • fertility preservation
  • Infertility

Name

Location

University Reproductive AssociatesHasbrouck Heights, New Jersey  07604