Status:
UNKNOWN
Oocyte Cryopreservation: Evaluation of an Oocyte Freezing and Thawing Technique
Lead Sponsor:
West Coast Fertility Centers
Conditions:
Infertility
Eligibility:
FEMALE
21-45 years
Brief Summary
Over the past several decades, considerable effort has been expended toward the successful cryopreservation of various human cells. While attempts at cryopreservation have been directed at different t...
Eligibility Criteria
Inclusion
- To be eligible for inclusion into this study, each subject must satisfy the following criteria:
- Infertile woman wishing to conceive and whose physician has recommended that she undergo IVF.
- Participants must be aged 21 to 35 years
- Body mass index (BMI) \< 38.
- Serum results for cycle day 3 FSH \<10 mIU/ml.
- Must have male partner whose semen analysis meets the clinic criteria for ICSI. Use of donor sperm is also acceptable.
- Be willing and able to comply with the protocol for the duration of the study.
- Have voluntarily provided written informed consent under WIRB, prior to any study-related procedure that is not part of normal medical care, with the understanding that the subjects may withdraw consent before they start Lupron without prejudice to their future medical care.
Exclusion
- A patient may NOT be entered into the study if she presents with ANY of the following criteria:
- Clinically significant systemic disease.
- Known endometriosis Grade III - IV (ASRM classification).
- Any previous cycle indicating a low response to gonadotropin stimulation (defined as retrieval of \< 10 eggs at retrieval)
- Three or more previous ART cycles without a clinical pregnancy
- Abnormal, undiagnosed, gynecological bleeding.
- Previous ovarian surgery
- Known allergy or hypersensitivity to recombinant gonadotropin preparations or any other study-related medications.
- Known current substance abuse.
- Simultaneous participation in another clinical trial.
- Current smoker.
- An extrauterine pregnancy within the last 3 months before OCP treatment commences.
- Previous participation in similar study at different centers.
Key Trial Info
Start Date :
April 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
April 1 2011
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00713869
Start Date
April 1 2006
End Date
April 1 2011
Last Update
January 6 2011
Active Locations (1)
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1
West Coast Fertility Centers
Fountain Valley, California, United States, 92708