Pediatric Cancer Clinical Trial
Official title:
Ovarian Tissue Cryopreservation for Fertility Preservation in Post-Pubertal Children Facing a Fertility Threatening Diagnosis or Treatment Regimen
NCT number | NCT05309746 |
Other study ID # | 2017-1149 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | November 1, 2017 |
Est. completion date | January 2035 |
The purpose of this study is to safely remove ovarian tissue in pediatric patients, who are at risk for infertility from their medical treatment, for freezing for future restoration of fertility and hormone function.
Status | Recruiting |
Enrollment | 250 |
Est. completion date | January 2035 |
Est. primary completion date | December 2030 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A to 30 Years |
Eligibility | Inclusion Criteria: - Post-pubertal individuals < 30 years of age - Will undergo imminent surgery, chemotherapy or radiation therapy that has implications on future fertility and reproductive hormone potential: any health condition or malignancy that requires removal of all or part of one or both ovaries, whole abdomen or pelvic irradiation= 10Gy in post-pubertal girls or =15 Gy in pre- pubertal girls - total body irradiation, and - alkylating-intensive chemotherapy - cyclophosphamide cumulative dose =7.5 g/m2 - any treatment regimen containing procarbazine - busulfan cumulative dose >600 mg/m2 - alkylating chemotherapy conditioning prior to stem cell transplantation - combination of any alkylating agent with total body irradiation or whole abdomen or pelvic radiation - cranial radiation =30 Gy - summed alkylating agent dose score =3 (Green et al., 2009) - cyclophosphamide equivalent dose (CED) = 4,000 mg/m2 (Green et al., 2014) - Patients may have newly diagnosed or relapsed disease. Those who were not enrolled at diagnosis are eligible even if they have received therapy that is viewed as likely to result in complete and permanent loss of ovarian function. However, these patients will be required to provide a 4mm punch biopsy of their tissue for research. Exclusion Criteria: - Patients with no anticipated oncologic therapies - Pregnant children - Children with one ovary - Children deemed high risk for perioperative complications - Patients unable to provide consent/assent (i.e. significant psychiatric problems/cognitive delay) |
Country | Name | City | State |
---|---|---|---|
United States | Ann &Robert H Lurie Children's Hospital | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
Erin Rowell |
United States,
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* Note: There are 32 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ovarian Tissue Freezing for Fertility Preservation in Post-Pubertal Children Facing a Fertility Threatening Medical Diagnosis or Treatment Regimen | Most of surgically removed tissue will be stored for the child's future use. Participants have the option of donating for research purposes a small piece of the ovarian tissue, a small amount of the child's blood and the media used to process the ovarian tissue (which is otherwise discarded, for research which evaluates optimizing ovarian cryopreservation and fertility restoration techniques. | 3 months | |
Secondary | Annual survey follow-up for participants who undergo ovarian tissue cryopreservation | The research study coordinator will contact families by email or telephone once per year and ask a series of questions related to ovarian function, such as frequency of menstruation. | yearly for up to 20 years |
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