Porst Hartmut, Sharlip Ira D, Hatzichristou Dimitris, Rubio-Aurioles Eusebio, Gittelman Marc, Stancil Britt-Nicole, Smith Peter M, Wilkins H Jeffrey, Pommerville Peter
Urological Practice, Hamburg, Germany.
Eur Urol. 2006 Nov;50(5):1086-94; discussion 1094-5. doi: 10.1016/j.eururo.2006.05.036. Epub 2006 Jun 8.
This study explored the efficacy of vardenafil in men with erectile dysfunction (ED) when taken 8 hours before sexual intercourse.
A 10-week, randomized, double-blind, placebo-controlled, parallel-group, flexible-dose study of vardenafil (5, 10 or 20mg) was conducted in men with ED for >6 months who failed >or=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.
383 patients were randomized to vardenafil (n=194) or placebo (n=189). Patients treated with vardenafil 8 hours before sexual activity achieved clinically meaningful (>or=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.
The extended duration of efficacy of vardenafil up to 8 hours postdose may provide couples with more flexibility in their sexual life than anticipated.
本研究探讨伐地那非在性交前8小时服用时对勃起功能障碍(ED)男性的疗效。
对患有ED超过6个月且在4周无治疗导入期内性交尝试失败≥50%的男性进行了一项为期10周的随机、双盲、安慰剂对照、平行组、灵活剂量的伐地那非(5、10或20mg)研究。性接触概况问题3(SEP3)是主要疗效指标;次要指标包括SEP2、国际勃起功能指数-勃起功能(IIEF-EF)领域评分、总体评估问题(GAQ)、总体信心问题(GCQ)和勃起质量量表(EQS)。全程进行不良事件和安全性监测。
383例患者被随机分为伐地那非组(n = 194)或安慰剂组(n = 189)。与接受安慰剂的患者相比,在性活动前8小时服用伐地那非的患者在第2至10周的临床意义上(≥18%)且统计学上显著更高的每位患者SEP3和SEP2成功率(SEP3为69%对34%;SEP2为81%对51%;均p<0.001)。从第2周起,SEP3和SEP2测量显示伐地那非比安慰剂具有显著优越性(p<0.001)。IIEF-EF领域评分、GAQ、GCQ和EQS的测量表明,与安慰剂相比,伐地那非导致勃起功能有显著更大的改善(所有p<0.001)。伐地那非总体耐受性良好。
伐地那非给药后长达8小时的延长疗效持续时间可能为夫妻在性生活中提供比预期更大的灵活性。