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Ovarian Tissue Cryopreservation in Females Undergoing Procedures That Will Potentially Lead To Loss of Ovarian Function

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01993732
Enrollment
15
Registered
2013-11-25
Start date
2013-08-06
Completion date
2018-06-28
Last updated
2019-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Auto Immune Disease, Cancer, Effects of Chemotherapy, Unspecified Complication of Bone Marrow Transplant

Keywords

Cancer, Cryopreservation, Ovarian Function, In Vitro

Brief summary

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.

Detailed description

The aim of this preliminary study is to retrieve and properly cryopreserve ovarian tissue for autotransplantation in any premenopausal female whose ovarian function is threatened in a physiological, pathological or iatrogenic manner in an effort to observe the return of ovarian endocrine function and development of egg(s) appropriate for use in in vitro fertilization.

Interventions

PROCEDURERetrieval and Cryopreservation

Females undergoing therapeutic procedures that will potentially lead to the irreversible loss of ovarian function will have their ovarian tissue retrieved and cryopreserved. Ideally, after treatment, the cryopreserved ovarian tissue can be thawed and auto-transplanted and ovarian function resumed.

Sponsors

Medical College of Wisconsin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
3 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Return of hormones produced by the ovarian tissue3 months after re-implantation

Secondary

MeasureTime frame
Development of egg(s) appropriate for use in in vitro fertilizationParticipants will be followed through their reproductive years (until the patient reaches 45 years of age)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026