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Recruiting NCT02872532

NCT02872532 Testicular Tissue Cryopreservation in Children

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Clinical Trial Summary
NCT ID NCT02872532
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition Cancer
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2016-08-16
Primary Completion 2030-12

Eligibility & Interventions

Sex Male only
Min Age 0 Years
Max Age 17 Years
Study Type INTERVENTIONAL
Interventions
Testicular tissue cryopreservation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 200 participants in total. It began in 2016-08-16 with a primary completion date of 2030-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This protocol is being designed to offer testicular tissue cryopreservation to male pediatric patients (0-17 years of age) with fertility threatening medical diagnoses or facing surgery, chemotherapy or radiation therapy that may cause loss of reproductive potential.

Eligibility Criteria

Inclusion Criteria: (All inclusion criteria must be met.) * Be male 0-17 years of age * Meet at least one of the following four conditions: * Be scheduled to undergo surgery, chemotherapy, drug treatment and/or radiation for the treatment or prevention of a medical condition or malignancy with risk of causing permanent and complete loss of subsequent testicular function. Risk categories based on treatment regimens are indicated below. Investigators will utilize three sources to calculate risk: 1. "Fertile Hope - Risks of Azoospermia" brochure that details typical agents and treatment regimens in each risk category, 2. The Summed Alkylating Agent dose score (Green et al., 2009) or 3. The Cyclophosphamide Equivalent Dose method (Green et al., 2014). Because of the complexity of many treatment regimens, patient risk categorization will be at the discretion of the investigators. * High Risk * \>= 80% risk of prolonged azoospermia, Fertile Hope Brochure * Summed alkylating agent dose score \>= 3 * Cyclophosphamide equivalent dose \>= 7,500mg/m\^2 * Intermediate risk (21-79% risk of prolonged azoospermia, Fertile Hope) * Low Risk ( =\< 20% risk of prolonged azoospermia, Fertile Hope) * Eligibility is limited to patients in the High risk category and/or intermediate risk after discussion with pediatric oncology, fertility preservation team, and the patient/family * Or, have a medical condition or malignancy that requires removal of all or part of one or both testicles * Or, have a medical condition (genetic or autoimmune) that results in decline in fertility (e.g. Klinefelter syndrome) * Or, have a newly diagnosed or recurrent disease affecting fertility. Those who were not enrolled at the time of initial diagnosis (i.e. patients with recurrent disease) are eligible if they have not previous received therapy that is viewed as likely to result in complete and permanent loss of testicular function * Have two testicles if undergoing elective removal of a testicle for fertility preservation only. Note: removal of both testicles will limit fertility preservation options. Or have 1 testicle but limited potential for future fertility due to underlying condition, malignancy, prior surgery or previous torsion and no other fertility preservation methods are available except for testicular tissue cryopreservation * Sign an approved informed consent and authorization permitting the release of personal health information. The patient and/or the patient's legally authorized guardian must acknowledge in writing that consent for specimen collection has been obtained, in accordance with institutional policies approved by the United States (U.S.) Department of Health and Human Services * Consent for serum screening tests for infectious diseases to be performed at the time of testicular tissue harvesting. The immediate testing will include but not be limited to testing for Hepatitis B, Hepatitis C, and human immunodeficiency virus (HIV) * Undergo a full history and physical examination and obtain standard pre-operative clearance (based on the most recent American College of Cardiology/ American Heart Association \[ACC/AHA\] Guideline for Perioperative Cardiovascular Evaluation for Noncardiac Surgery) as determined by their primary surgeon * Note: In cases of torsion of testicles or other medical conditions that result in impairment of testicular function, patients can be consented and included in the study, if during the testicular surgery the provider finds that the patient still has viable tissue that can be cryopreserved. Exclusion Criteria: (Any exclusion criteria will disqualify.) * Diagnosed with psychological, psychiatric, or other conditions which prevent giving fully informed consent. * Diagnosed with an underlying medical condition that significantly increases their risk of complications from anesthesia and surgery. * Previous recipients of gonadotoxic chemotherapy or radiation therapy thought to have resulted in impairment of testicular function.

Contact & Investigator

Central Contact

Asma Chattha, MBBS

✉ chattha.asma@mayo.edu

📞 507-538-0127

Principal Investigator

Candace F. Granberg, MD

PRINCIPAL INVESTIGATOR

Mayo Clinic in Rochester

Frequently Asked Questions

Who can join the NCT02872532 clinical trial?

This trial is open to male participants only, aged 0 Years or older, up to 17 Years, studying Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT02872532 currently recruiting?

Yes, NCT02872532 is actively recruiting participants. Contact the research team at chattha.asma@mayo.edu for enrollment information.

Where is the NCT02872532 trial being conducted?

This trial is being conducted at Rochester, United States.

Who is sponsoring the NCT02872532 clinical trial?

NCT02872532 is sponsored by Mayo Clinic. The principal investigator is Candace F. Granberg, MD at Mayo Clinic in Rochester. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology