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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01178463
Other study ID # HYMC-0065-09
Secondary ID
Status Active, not recruiting
Phase N/A
First received August 9, 2010
Last updated August 9, 2010
Start date January 2010
Est. completion date October 2010

Study information

Verified date August 2010
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

The researchers hypothesized that nonobstructive azoospermia might be associated with a reduction OF SSCs in seminiferous tubules as compared with obstructive azoospermia. Testicular sperm specimens that had been previously extracted from azoospermic patients will be paraffin embedded and stained with anti GPR-125. After antigen retrieval, the sections will be incubated with rabbit anti GPR125 followed by Cy3-conjugated anti rabbit secondary antibodies. Those found to be SSCs will be counted using light microscopy, and compared between patients with obstructive (n=11) and non-obstructive azoospermia (n=9).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 25
Est. completion date October 2010
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Male
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Azoospermic patients

Exclusion Criteria:

- Patients with sperm cells

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Other:
Biospecimen staining
The sections will be incubated with rabbit anti GPR125 followed by Cy3-conjugated anti rabbit secondary antibodies.
Biospecimen staining
The sections will be incubated with rabbit anti GPR125 followed by Cy3-conjugated anti rabbit secondary antibodies.

Locations

Country Name City State
Israel Hillel Yaffe Medical Center - IVF Unit Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary SSCs were identified in both obstructive and nonobstructive azoospermia patients. One year No
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