Testicular Tissue Viability After Cryopreservation
The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2010 by Hadassah Medical Organization.
Recruitment status was Not yet recruiting
Recruitment status was Not yet recruiting
Sponsor:
Hadassah Medical Organization
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01262495
First received: December 16, 2010
Last updated: NA
Last verified: December 2010
History: No changes posted
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Purpose
we will use testicular tissue from patient who underwent orchidectomy due to medical reasons and test the viability of the tissue after cryopreservation and de-freezing.
| Condition | Intervention |
|---|---|
|
Fertility |
Other: cryopreservation |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Supportive Care |
Further study details as provided by Hadassah Medical Organization:
Primary Outcome Measures:
- viable tissue after cryopreservation [ Time Frame: 1/1/2011 - 30/12/2012 ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 5 |
| Study Start Date: | January 2011 |
| Estimated Study Completion Date: | December 2011 |
| Estimated Primary Completion Date: | December 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
orchidectomy
as specified in the summary
|
Other: cryopreservation
cryopreservation of testicular tissue
|
Eligibility| Ages Eligible for Study: | 15 Years to 75 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria: male patient undergo orchidectomy -
Exclusion Criteria: non viable testicular tissue
-
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01262495
Contacts
| Contact: Doron Kabiri, MD | 972-508946898 | doronlilach@gmail.com |
Locations
| Israel | |
| Hadassah Medical Organization | Not yet recruiting |
| Jerusalem, Israel | |
| Contact: hadassah 0508946898 | |
| Principal Investigator: Doron Kabiri, MD | |
Sponsors and Collaborators
Hadassah Medical Organization
More Information
No publications provided
| Responsible Party: | hadassah |
| ClinicalTrials.gov Identifier: | NCT01262495 History of Changes |
| Other Study ID Numbers: | kabiri HMO-CTIL |
| Study First Received: | December 16, 2010 |
| Last Updated: | December 16, 2010 |
| Health Authority: | Israel: Ethics Commission |
ClinicalTrials.gov processed this record on June 18, 2013