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Sponsored by: |
Pfizer |
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Information provided by: | Pfizer |
ClinicalTrials.gov Identifier: | NCT00159848 |
This study will demonstrate if a treatment optimization program has an impact on the satisfaction with Viagra treatment in men with erectile dysfunction
Condition | Intervention | Phase |
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Impotence |
Behavioral: Treatment Optimization Program (educational material) |
Phase IV |
Study Type: | Interventional |
Study Design: | Educational/Counseling/Training, Non-Randomized, Open Label, Uncontrolled, Crossover Assignment, Efficacy Study |
Official Title: | Effectiveness Of An Educational Program To Improve Patients' Satisfaction Regarding Their Management Of Erectile Dysfunction With Sildenafil |
Estimated Enrollment: | 8000 |
Study Start Date: | September 2003 |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Male |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | NRA1481115 |
Study First Received: | September 8, 2005 |
Last Updated: | October 26, 2005 |
ClinicalTrials.gov Identifier: | NCT00159848 History of Changes |
Health Authority: | Canada: Health Canada |
Sexual Dysfunctions, Psychological Sexual Dysfunction, Physiological Mental Disorders |
Sildenafil Genital Diseases, Male Erectile Dysfunction |
Sexual Dysfunctions, Psychological Sexual Dysfunction, Physiological Mental Disorders |
Genital Diseases, Male Sexual and Gender Disorders Erectile Dysfunction |