Cancer Clinical Trial
Official title:
Ovarian Tissue Cryopreservation As A Means Of Preserving Ovarian Function in Females Undergoing Therapeutic Procedures That Will Potentially Lead To The Irreversible Loss of Ovarian Function
NCT number | NCT01993732 |
Other study ID # | 126204 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 6, 2013 |
Est. completion date | June 28, 2018 |
Verified date | August 2019 |
Source | Medical College of Wisconsin |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to retrieve and cryopreserve ovarian tissue from females undergoing a treatment that may lead to irreversible loss of ovarian function.
Status | Completed |
Enrollment | 15 |
Est. completion date | June 28, 2018 |
Est. primary completion date | June 28, 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 3 Years and older |
Eligibility |
Inclusion Criteria: - Patient must be female. - Patient must have a disease process where the disease or its treatment adversely affects ovarian function. - Patient must be recommended for this study by their oncologist or specialist. - Patient (or legally authorized representative) must sign an informed consent. Exclusion Criteria: - Patients cannot be male. - Patients must not be HIV positive. - Patient cannot have a poor diagnosis such that she is not expected to survive to adulthood. - Patient cannot have any medical condition that would contraindicate surgery. - Patient cannot have any medical condition that would contraindicate general anesthesia. - Patient cannot have any medical condition that would contraindicate pregnancy. |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital of Wisconsin | Milwaukee | Wisconsin |
United States | Froedtert and The Medical College of Wisconsin | Milwaukee | Wisconsin |
Lead Sponsor | Collaborator |
---|---|
Medical College of Wisconsin |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Return of hormones produced by the ovarian tissue | 3 months after re-implantation | ||
Secondary | Development of egg(s) appropriate for use in in vitro fertilization | Participants will be followed through their reproductive years (until the patient reaches 45 years of age) |
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