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Clinical Trial Summary

Erectile dysfunction will be explored by recording R / P and self-administered questionnaire IIEF-5.


Clinical Trial Description

Erectile dysfunction will be explored by recording R / P and self-administered questionnaire IIEF-5. This dual evaluation will be made before the beginning of the therapeutic treatment and 3 months and 12 months after surgery. Assessed by IIEF-5 will be made only 6, 18 and 24 months after surgery. There will be no changes made to support oncology patients. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT01843218
Study type Interventional
Source Institut Bergonié
Contact
Status Terminated
Phase N/A
Start date March 2008
Completion date December 2015

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