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Clinical Trial Summary

Determine safety and effectiveness of the technique using autologous stem cells in the treatment of urinary incontinence in one male subject.


Clinical Trial Description

Autologous stem cells will be obtained from the subject by needle biopsy, sent to a lab for multiplication and after about 6 weeks time will be injected into the subjects urethra. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01648491
Study type Interventional
Source William Beaumont Hospitals
Contact
Status Active, not recruiting
Phase N/A
Start date March 2011
Completion date June 2016

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