Secondary Infertility Clinical Trial
Official title:
Surgical Ovarian Preservation in Females Undergoing Chemo-Radiotherapy
NCT number | NCT02429349 |
Other study ID # | 13-02542-FB |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 2015 |
Est. completion date | June 30, 2020 |
Verified date | November 2020 |
Source | University of Tennessee |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to assess the results of ovarian tissue freezing, such as resumption or initiation of menses (menstruation: the discharge of blood and tissue from the uterus that happens about every 4 weeks in females who are not pregnant) and pregnancy, prior to starting chemotherapy or radiation treatment (commonly used for cancer treatment or for other conditions such as multiple sclerosis, psoriasis, rheumatoid arthritis). Females who are about to undergo chemotherapy or radiation therapy for cancer or these other medical conditions may stop having menses and may not be able to produce a biological child. Girls who have not achieved puberty and are exposed to chemotherapy (alkylating agents) or radiation treatment, the risk is up to 22-50%. In contrast, girls older than 10 years, or who have achieved puberty, experience acute ovarian failure in over 50% of the cases. By freezing and preserving ovarian tissue will help prevent these outcomes. In fact, when you are considered cured of your disease, you will have another surgical procedure where your own ovarian tissue will be transplanted back to you. This surgery will increase the possibility of resuming/initiating menses and the chance to have a pregnancy.
Status | Completed |
Enrollment | 2 |
Est. completion date | June 30, 2020 |
Est. primary completion date | March 30, 2020 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 8 Years to 40 Years |
Eligibility | Inclusion Criteria: 1. Pre- and post-pubertal patients who are diagnosed with conditions that necessitate chemo- or radiotherapy and wish to preserve their ovarian function. Exclusion criteria: 1. Patients with acute or chronic conditions that would preclude surgery. These include, but are not limited to, hyper- or hypo-coagulation disorders, lung conditions precluding mechanical ventilation, brain death. 2. Patients for whom the primary oncologist and/or pathologist discourage entering the protocol because of specific condition characteristics. These include, but are not limited to, cancers with high risk of ovarian metastasis such as leukemia and non-Hodgkin lymphoma. 3. Patients with known positive bone marrow for leukemia or solid tumor. 4. Patients whose tumor is in an organ that communicates with the peritoneum and peritoneal sampling at time of primary excision shows evidence of disease. 5. Patients older than 40 years of age. 6. Males. |
Country | Name | City | State |
---|---|---|---|
United States | Methodist/LeBonheur Hospital | Germantown | Tennessee |
United States | Baptist Memorial Hospital | Memphis | Tennessee |
United States | LeBonheur Children's Hospital | Memphis | Tennessee |
United States | Methodist University Hospital | Memphis | Tennessee |
United States | Regional One Health Ob-Gyn Clinic | Memphis | Tennessee |
United States | Regional One Health, Regional Medical Center, Operating Room | Memphis | Tennessee |
United States | St. Jude Children's Research Hospital | Memphis | Tennessee |
Lead Sponsor | Collaborator |
---|---|
University of Tennessee |
United States,
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* Note: There are 49 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Comparison of biochemical markers, i.e., Estradiol, FSH; LH, AMH; Inhibin B | Evaluation of biometry and of specific biochemical markers in the serum before and after chemo/radiation treatment and ovarian tissue explant, and in ovarian samples. | Follow-up at stated intervals, up to 30 years | |
Primary | Resumption of menses | Timing for resumption menses- patient report, physical evaluation at stated intervals. | Post-op, after initial explant surgery, & one month after, & every 6-12 months until autotransplant of tissue; through 40 yrs of age/menopause (or, pt.decision to stop earlier) | |
Primary | Initiation of menses | Timing for initiation of menses- patient report, physical evaluation at stated intervals | Post-op, after initial explant surgery, & one month after, & every 6-12 months until autotransplant of tissue; through 40 yrs of age/menopause (or, pt.decision to stop earlier) | |
Primary | Completion of puberty | Timing for completion of puberty - patient report, physical evaluation at stated intervals | Post-op, after initial explant surgery, & one month after, & every 6-12 months until autotransplant of tissue; through 40 yrs of age/menopause (or, pt.decision to stop earlier) | |
Primary | Fertility | Timing for initiation of pregnancy - patient report, physical evaluation at stated intervals | Post-op, after initial explant surgery, & one month after, & every 6-12 months until autotransplant of tissue; through 40 yrs of age/menopause (or, pt.decision to stop earlier) | |
Secondary | Physical UTERINE development | Physical assessment and pelvic ultrasound to evaluate uterine development before and after chemo- or radiotherapy treatment. Lifespan of transplanted cortex function (patient follow-up). | Follow-up at stated intervals, up to 30 years | |
Secondary | Physical OVARIAN development | Physical assessment and pelvic ultrasound to evaluate ovarian development before and after chemo- or radiotherapy treatment. Lifespan of transplanted cortex function (patient follow-up). | Follow-up at stated intervals, up to 30 years |
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