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Assess Efficacy in Subjects With Traumatic Spinal Cord Injury — LEMDE  

Spinal Cord Injury Clinical Trial

Official title:
Double-blind, Cross-over, Placebo Controlled Pilot Study to Characterize the Profile of Those Patients With Spinal Cord Injury Diagnosed by Electrophysiological, Urodynamic and Clinical (ASIA Group) Assessment Who May Respond to Vardenafil Treatment. (LEMDE)

Clinical Trial Summary

Assess efficacy of Vardenafil in patients with traumatic spinal cord injury

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00667966
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 4
Start date July 2005
Completion date February 2007
View Details
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