Status:
TERMINATED
Real Life Safety and Efficacy of Vardenafil
Lead Sponsor:
Bayer
Conditions:
Erectile Dysfunction
Eligibility:
MALE
18+ years
Brief Summary
In this uncontrolled, non-randomized, prospective, local post-marketed surveillance study, data are obtained on safety and efficacy of LEVITRA® in routine treatment of erectile dysfunction. The genera...
Eligibility Criteria
Inclusion
- Any adult patient (\>/=18 years) with erectile dysfunction treated with LEVITRA®.
- Patients must be able to give written informed consent for participation in the study after receiving detailed written and oral information prior to the study.
Exclusion
- Exclusion criteria must be read in conjunction with the product information (Package Insert).
Key Trial Info
Start Date :
February 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
November 1 2008
Estimated Enrollment :
372 Patients enrolled
Trial Details
Trial ID
NCT01215409
Start Date
February 1 2008
End Date
November 1 2008
Last Update
May 19 2014
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Many Locations, Taiwan