CLINICAL PROTOCOL A PROSPECTIVE MULTICENTER, PARALLEL GROUP STUDY WITH A SINGLE BLIND PHASE AND A DOUBLE BLIND RANDOMISED PHASE, TO EVALUATE THE EFFICACY AND SATISFACTION OF VIAGRA (SILDENAFIL CITRATE) HIGH DOSE (100MG) TITRATION COMPARED WITH 50MG DOSE, IN MEN WITH ERECTILE DYSFUNCTIO
- Conditions
- Erectile DysfunctionMedDRA version: 6.1Level: PTClassification code 10061461
- Registration Number
- EUCTR2005-002411-25-IT
- Lead Sponsor
- PFIZER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Male
- Target Recruitment
- 500
Inclusion Criteria
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: ;Secondary Objective: ;Primary end point(s):
- Secondary Outcome Measures
Name Time Method