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Spermatogonial Stem Cell (SSC) Transplant and Testicular Tissue Grafting

Primary Purpose

Infertility, Male, Cancer, Autoimmune Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Spermatogonial Stem Cell Transplant and Testicular Tissue Grafting
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility, Male focused on measuring spermatogonial stem cells, testis, fertility, oncofertility

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male participant at least in Tanner stage 3
  • Previously cryopreserved and stored testicular tissue/cells (frozen due to an infertility-risking diagnosis or treatment such as chemotherapy or radiation) available for autologous transplantation and grafting
  • Healthy enough to undergo anesthesia
  • Written clearance for the procedure from the patient's hematologist or oncologist to confirm the patient has finished treatment for primary condition and are clear to undergo autologous stem cell transplant

Exclusion Criteria:

  • Participants considered to be high risk for surgical complications
  • Participants with a history of leukemia, lymphoma or testicular cancer or a cancer that likely involved testicles at the time of testicular tissue collection
  • Diagnosed with psychological, psychiatric, or other conditions which prevent giving fully informed consent.

Sites / Locations

  • Magee-Womens HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Spermatogonial Stem Cell Transplant & Testicular Tissue Graft

Arm Description

Stem cell transplantation Testicular tissue grafting

Outcomes

Primary Outcome Measures

Number of participants with return of spermatogenesis
Rate of participants where sperm was found in semen analysis or testicular tissue analysis

Secondary Outcome Measures

Number of participants with cancer recurrence
Rate of participants diagnosed with cancer recurrence
Number of participants with surgical complications of SSC transplantation and testicular tissue grafting
Rate of infection, hospital readmission, re-operation occurs

Full Information

First Posted
June 18, 2020
Last Updated
October 4, 2023
Sponsor
University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT04452305
Brief Title
Spermatogonial Stem Cell (SSC) Transplant and Testicular Tissue Grafting
Official Title
Spermatogonial Stem Cell (SSC) Transplant and Testicular Tissue Grafting
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 2023 (Anticipated)
Primary Completion Date
July 1, 2025 (Anticipated)
Study Completion Date
July 1, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Spermatogonial stem cell transplantation through ultrasound guided rete testis injection and testicular tissue grafting will be performed for participants who have frozen testicular tissue prior to gonadotoxic therapy. The purpose of this study is to test the safety and feasibility of these transplant technologies and restore fertility for these participants.
Detailed Description
Azoospermia (no sperm in ejaculated semen) impacts 1% of men in the general population and 15% of infertile men, which translates to 645,000 males between the ages of 20 and 50 (prime reproductive years) in the United States. Spermatogenesis arises from a population of spermatogonial stem cells in the testes that maintain continuous sperm production throughout a man's post-pubertal life. Diseases or medical treatments that compromise the stem cell pool and/or prevent the stem cells from differentiating can cause infertility. Adult men have the option to cryopreserve a semen sample prior to therapy but this is not an option for prepubertal patients who are not yet producing sperm. This study will test the safety and feasibility of two approaches to restore sperm production using previously cryopreserved testicular tissues, which contain spermatogonial stem cells. The first approach is autologous transplantation of testicular cells, including spermatogonial stem cells, into the testis using ultrasound-guided rete testis injection. The second approach is autologous grafting of intact pieces of testicular tissue under the skin in the scrotum.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Male, Cancer, Autoimmune Disorder
Keywords
spermatogonial stem cells, testis, fertility, oncofertility

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Spermatogonial Stem Cell Transplant & Testicular Tissue Graft
Arm Type
Experimental
Arm Description
Stem cell transplantation Testicular tissue grafting
Intervention Type
Procedure
Intervention Name(s)
Spermatogonial Stem Cell Transplant and Testicular Tissue Grafting
Intervention Description
Spermatogonial stem cell transplant and testicular tissue grafting is performed to produce sperm.
Primary Outcome Measure Information:
Title
Number of participants with return of spermatogenesis
Description
Rate of participants where sperm was found in semen analysis or testicular tissue analysis
Time Frame
3 months-1year
Secondary Outcome Measure Information:
Title
Number of participants with cancer recurrence
Description
Rate of participants diagnosed with cancer recurrence
Time Frame
5 years
Title
Number of participants with surgical complications of SSC transplantation and testicular tissue grafting
Description
Rate of infection, hospital readmission, re-operation occurs
Time Frame
3 months

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male participant at least in Tanner stage 3 Previously cryopreserved and stored testicular tissue/cells (frozen due to an infertility-risking diagnosis or treatment such as chemotherapy or radiation) available for autologous transplantation and grafting Healthy enough to undergo anesthesia Written clearance for the procedure from the patient's hematologist or oncologist to confirm the patient has finished treatment for primary condition and are clear to undergo autologous stem cell transplant Exclusion Criteria: Participants considered to be high risk for surgical complications Participants with a history of leukemia, lymphoma or testicular cancer or a cancer that likely involved testicles at the time of testicular tissue collection Diagnosed with psychological, psychiatric, or other conditions which prevent giving fully informed consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rachel Neelley
Phone
412-641-7475
Ext
1
Email
fertilitypreservation@upmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kyle E Orwig, PhD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Magee-Womens Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rachel Neelley
Phone
412-641-7475
Ext
1
Email
fertilitypreservation@upmc.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
The investigators will publish individual participant data, after deidentification. The investigators will also report each individual participants data back to them. Participants will be identified with unique ID numbers. No identifiable information will be shared.
IPD Sharing Time Frame
Beginning 9 months and ending 36 months following article publication.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal. Proposals should be directed at korwig@mwri.magee.edu

Learn more about this trial

Spermatogonial Stem Cell (SSC) Transplant and Testicular Tissue Grafting

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