Satisfaction With Phosphodiesterase 5 Inhibitors Treatment In Patients With Cardiovascular Risk
NCT00874185
Last updated date
ABOUT THIS STUDY
Evaluate satisfaction in people treated with IPDE5 inhibitors over time
FOR MORE INFORMATION
Contact a representative by phone, email, or visiting the study website. Please see the references below:
By phone
Pfizer Clinical Trials Contact Center
1-800-718-1021
Eligibility Criteria
condition
Erectile Dysfunction
Sex
Male
Age
18 + years
Inclusion Criteria
Show details
- CV risk factors
- Male above 18
Exclusion Criteria
Show details
- Non-informed consent
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Advanced Information
Descriptive Information | ||||
---|---|---|---|---|
Brief Title | Satisfaction With Phosphodiesterase 5 Inhibitors Treatment In Patients With Cardiovascular Risk | |||
Official Title | Satisfaction With Treatment In Patients With Erectile Dysfunction And Cardiovascular Risk And/Or Previous Cardiovascular Event. | |||
Brief Summary | Evaluate satisfaction in people treated with IPDE5 inhibitors over time | |||
Detailed Description | 12 first patients that are eligible | |||
Study Type | Observational | |||
Study Design | Observational Model: Cohort Time Perspective: Prospective | |||
Target Follow-Up Duration | Not Provided | |||
Biospecimen | Not Provided | |||
Sampling Method | Non-Probability Sample | |||
Study Population | People with cv risk | |||
Condition | Erectile Dysfunction | |||
Intervention | Not Provided | |||
Study Groups/Cohorts | Questionnaire
filling in questionnaires | |||
Publications * | Not Provided | |||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. | ||||
Recruitment Information | ||||
Recruitment Status | Completed | |||
Actual Enrollment | 720 | |||
Original Actual Enrollment | 572 | |||
Actual Study Completion Date | May 2008 | |||
Actual Primary Completion Date | May 2008 (Final data collection date for primary outcome measure) | |||
Eligibility Criteria | Inclusion Criteria:
Exclusion Criteria:
| |||
Sex/Gender |
| |||
Ages | 18 Years and older (Adult, Older Adult) | |||
Accepts Healthy Volunteers | No | |||
Contacts | Contact information is only displayed when the study is recruiting subjects | |||
Listed Location Countries | Not Provided | |||
Removed Location Countries | ||||
Administrative Information | ||||
NCT Number | NCT00874185 | |||
Other Study ID Numbers | A1481256 A1481256 | |||
Has Data Monitoring Committee | No | |||
U.S. FDA-regulated Product | Not Provided | |||
IPD Sharing Statement | Not Provided | |||
Responsible Party | Pfizer | |||
Study Sponsor | Pfizer | |||
Collaborators | Not Provided | |||
Investigators |
| |||
PRS Account | Pfizer | |||
Verification Date | February 2013 |