Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Recruiting NCT05309746

Ovarian Tissue Cryopreservation in Post Pubertal (OTC-Post Pubertal)

Conditions: Pediatric Cancer

Sex: Female
Ages: N/A – 30 Years
Healthy volunteers: No
Enrollment: 250
Sponsor: Erin Rowell

Location: Ann &Robert H Lurie Children's Hospital Chicago Illinois

Summary

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.

Eligibility Criteria

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)

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05309746). StuddyBuddy aggregates publicly available trial information.