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Testicular Tissue Viability After Cryopreservation

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ClinicalTrials.gov Identifier: NCT01262495
Recruitment Status : Unknown
Verified December 2010 by Hadassah Medical Organization.
Recruitment status was:  Not yet recruiting
First Posted : December 17, 2010
Last Update Posted : December 17, 2010
Sponsor:
Information provided by:

Study Description
Brief Summary:
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 or disease Intervention/treatment
Fertility Other: cryopreservation

Study Design

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 5 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Study Start Date : January 2011
Estimated Primary Completion Date : December 2011
Estimated Study Completion Date : December 2011
Arms and Interventions

Arm Intervention/treatment
orchidectomy
as specified in the summary
Other: cryopreservation
cryopreservation of testicular tissue


Outcome Measures

Primary Outcome Measures :
  1. viable tissue after cryopreservation [ Time Frame: 1/1/2011 - 30/12/2012 ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   15 Years to 75 Years   (Child, Adult, Senior)
Sexes Eligible for Study:   Male
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria: male patient undergo orchidectomy -

Exclusion Criteria: non viable testicular tissue

Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

Responsible Party: hadassah
ClinicalTrials.gov Identifier: NCT01262495     History of Changes
Other Study ID Numbers: kabiri HMO-CTIL
First Posted: December 17, 2010    Key Record Dates
Last Update Posted: December 17, 2010
Last Verified: December 2010