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Clinical Trial Summary

To demonstrate the efficacy, safety and tolerability of sildenafil administered orally, as required, approximately 1 hour prior to sexual activity to men with erectile dysfunction (ED) associated with spinal cord injury (SCI), as well as its effects on the quality of life (QoL) of these patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00654082
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 4
Start date September 2002
Completion date August 2003

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