BAY38-9456 - Supportive Trial for Spinal Injury

Status Completed

Clinical Trial Summary

BAY 38-9456 10 mg and 20 mg can be given as safe and efficacious medications to patients with spinal cord injury suffering from erectile dysfunction, and that erectile dysfunction can be improved by uptitration to BAY 38-9456 20 mg when the treatment with 10 mg is not sufficiently effective

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00652262
Study type	Interventional
Source	Bayer
Contact
Status	Completed
Phase	Phase 3
Start date	March 2004
Completion date	November 2004

View Details

See also
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