Satisfaction With Phosphodiesterase 5 Inhibitors Treatment In Patients With Cardiovascular Risk
Completed
- Conditions
- Erectile Dysfunction
- Registration Number
- NCT00874185
- Lead Sponsor
- Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
- Brief Summary
Evaluate satisfaction in people treated with IPDE5 inhibitors over time
- Detailed Description
12 first patients that are eligible
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 720
Inclusion Criteria
- CV risk factors
- Male above 18
Exclusion Criteria
- Non-informed consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method EDITS 6 months SEAR 6 months
- Secondary Outcome Measures
Name Time Method Medication prescribed 6 months
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie PDE5 inhibitor efficacy in ED patients with cardiovascular risk factors?
How do PDE5 inhibitors compare to standard-of-care treatments for ED in post-cardiovascular event patients?
Which biomarkers correlate with treatment satisfaction in NCT00874185 cardiovascular ED cohort?
What adverse events are reported in PDE5 inhibitor use for ED patients with hypertension or atherosclerosis?
Are there combination therapies or competitor drugs improving outcomes for ED with cardiovascular comorbidities?