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Oocyte Cryopreservation

Weill Cornell Medicine (WCM) logo

Weill Cornell Medicine (WCM)

Status

Completed

Conditions

Fertility Preservation

Treatments

Procedure: Oocyte cryopreservation

Study type

Interventional

Funder types

Other

Identifiers

NCT01696786
0903010292

Details and patient eligibility

About

The specific aim of this study is to further develop methods of oocyte cryopreservation and evaluate their impact on reproductive outcomes.

Enrollment

250 estimated patients

Sex

Female

Ages

Under 42 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Any consenting female who wishes to freeze unfertilized oocytes and are:

  1. at risk for ovarian hyperstimulation syndrome (enlarged ovaries with abdominal fluid accumulation) and postponement of pregnancy has been recommended.
  2. a cancer patient anticipating treatment and have been cleared by the oncologists for ovarian stimulation.
  3. a female who seeks to preserve her future fertility and does not wish to use donor or partner sperm to fertilize her eggs.
  4. a donor egg recipient who elects to have some of the eggs obtained fertilized with husband/partner sperm and the rest cryopreserved for future use.
  5. a patient for whom the partner's sperm retrieval or production has failed and donor sperm is not an option.
  6. a patient who, for religious or ethical reasons, wants to limit the number of fresh oocytes exposed to sperm (fertilization) and do not want to either discard or donate the excess oocytes.

AND

  1. has been clinically and psychologically approved for ovarian stimulation
  2. age between 12 and 42 years, inclusive, at time of informed consent.
  3. willing and able to comply with the protocol.
  4. willing to provide follow-up information from her OB/GYN of any CVS/amniocentesis results, as well as information on obstetrical outcome.
  5. agree to undergo intracytoplasmic sperm injection (ICSI) when oocytes are thawed.

For cancer patients:

  1. No significant ovarian pathology as judged by physical exam and radiological studies;
  2. Patient's general condition and prognosis deemed favorable for surgery and chemo/radio therapy;
  3. No other major medical illness,
  4. Oncologist approval for the ovarian stimulation and egg retrieval.

Exclusion criteria

Age > 42 Subjects who do not meet the inclusion criteria will be ineligible for participation in this study.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

250 participants in 1 patient group

Oocyte cryopreservation
Experimental group
Treatment:
Procedure: Oocyte cryopreservation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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