Article ID Journal Published Year Pages File Type
3930078 European Urology 2006 10 Pages PDF
Abstract

ObjectivesThis study explored the efficacy of vardenafil in men with erectile dysfunction (ED) when taken 8 hours before sexual intercourse.MethodsA 10-week, randomized, double-blind, placebo-controlled, parallel-group, flexible-dose study of vardenafil (5, 10 or 20 mg) was conducted in men with ED for >6 months who failed ≥50% of intercourse attempts during a 4-week treatment-free run-in period. Sexual Encounter Profile Question 3 (SEP3) was the primary efficacy measure; secondary measures included SEP2, International Index of Erectile Function-Erectile Function (IIEF-EF) domain score, Global Assessment Question (GAQ), Global Confidence Question (GCQ) and Erection Quality Scale (EQS). Adverse-event and safety monitoring were conducted throughout.Results383 patients were randomized to vardenafil (n = 194) or placebo (n = 189). Patients treated with vardenafil 8 hours before sexual activity achieved clinically meaningful (≥18%) and statistically significantly greater least-squares mean per-patient SEP3 and SEP2 success rates over weeks 2–10, compared with patients receiving placebo (SEP3 69% vs 34%; SEP2 81% vs 51%; both p < 0.001). SEP3 and SEP2 measures demonstrated the significant superiority of vardenafil over placebo from week 2 onwards (p < 0.001). Measurements of IIEF-EF domain score, GAQ, GCQ and EQS showed that vardenafil led to significantly greater improvements in erectile function, compared with placebo (all p < 0.001). Vardenafil was generally well tolerated.ConclusionsThe extended duration of efficacy of vardenafil up to 8 hours postdose may provide couples with more flexibility in their sexual life than anticipated.

Related Topics
Health Sciences Medicine and Dentistry Obstetrics, Gynecology and Women's Health
Authors
, , , , , , , , ,