Oocyte Vitrification for In Vitro Fertilization (IVF) Patients and Women With Fertility Threatening Conditions

NCT ID: NCT01448460

Last Updated: 2013-01-24

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 8 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2009-09-30
• Study Completion Date: 2013-01-31

Brief Summary

Vitrification is a method of cryopreserving tissue for future use. It is widely used to preserve extra, good quality embryos generated from infertility treatments. It is becoming popular for the preservation of oocytes (eggs) as well, but is still considered investigational in this respect. The purpose of this study is to provide egg freezing for patients desiring fertility preservation. Although commonly used in clinics around the world, it should be offered as an IRB approved study procedure until it is no longer considered investigational by the American Society of Reproductive Medicine.

Conditions

Fertility Preservation

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Fertility Patients

IVF patients with extra eggs or other subjects who desire egg vitrification for fertility preservation

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Women between the ages of 18 and 37 and who require IVF for a successful pregnancy will be approached to consent for the study,. They must also have a cycle day 3 FSH < 10 mIU/ml, estradiol < 70 pg/ml and a baseline follicle count > 10. The BMI must be between 20 and 32kg/m2. If they do consent, eggs will only be vitrified if 13 or more mature metaphase II oocytes are collected.
• Women between the ages of 14 and 42 who are seeking treatment for fertility preservation. In addition they must also meet the following criteria.
• Patient is willing and able to delay any relevant therapy for up to 40 days.
• Have functioning ovaries as determined by blood / ultrasound testing.
• Patient is willing to undergo infectious disease testing for HIV, hepatitis B and C, syphilis, gonorrhea and Chlamydia.
• The patient must have clearance from their oncologist or medical specialist, if any, to undergo ovarian stimulation and transvaginal oocyte retrieval.
• The patient must not have a past history of blood clots in the veins or in the lungs.
• The patient must be willing to undergo transvaginal, internal ultrasound examination and pelvic examination.

Exclusion Criteria

• Patients with a cycle day 3 FSH > 10 mIU/ml, cycle day 3 estradiol > 70 pg/ml and a baseline follicle count < 10 will be excluded.
• Patients with a BMI <20 and >32 will be excluded.
• Patients who are not willing or are unable to meet the above mentioned eligibility requirments.
• Patients with expected low ovarian reserve [evaluated on day 3 by an antral follicle count of <3 follicles at 2-5 mm diameter and/or an increased concentration of follicle stimulating hormone (FSH) >15 IU [15] on cycle day 3 ].
• Patients with possible poor quality of oocytes, based on medical history including previous exposure to chemotherapeutics or radiation.

• Minimum Eligible Age: 14 Years
• Maximum Eligible Age: 42 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

University of Louisville

OTHER

Sponsor Role: lead

Responsible Party

Greg L. Christensen

IVF Lab Director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

09.356

Identifier Type: -

Identifier Source: org_study_id