Status:
COMPLETED
REPEAT - Real-Life Perception of Efficacy, Attitude, Satisfaction and Safety of Levitra Therapy
Lead Sponsor:
Bayer
Conditions:
Erectile Dysfunction
Eligibility:
MALE
18+ years
Brief Summary
The aim of this prospective, non-interventional post-marketing surveillance study is to obtain data on safety and efficacy of Levitra in routine treatment of erectile dysfunction. Furthermore, the dat...
Eligibility Criteria
Inclusion
- Outpatients with diagnosis of erectile dysfunction, decision taken by the investigator to prescribe Vardenafil.
Exclusion
- Exclusion criteria must be read in conjunction with the local product information. All contraindications listed in the local product information are applicable.
Key Trial Info
Start Date :
March 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2010
Estimated Enrollment :
7293 Patients enrolled
Trial Details
Trial ID
NCT00874679
Start Date
March 1 2007
End Date
April 1 2010
Last Update
November 11 2011
Active Locations (15)
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1
Many Locations, China
2
Many Locations, Croatia
3
Many Locations, France
4
Many Locations, Germany