Guo Ying-Lu, Viswanathan Vijay P, Chiang Han-Sun, Choi Hyung Ki, Yip Andrew Wai Chun, Shen Wei, Kopernicky Vladimir
Andrology Center, Peking University First Hospital, Peking University, Beijing 100009, China.
Asian J Androl. 2009 Jul;11(4):423-33. doi: 10.1038/aja.2009.11. Epub 2009 Apr 20.
We evaluated the efficacy and safety of as-needed tadalafil in a diverse clinical population (with varying patient demographics, disease severity, and comorbid medical conditions) of Asian men with erectile dysfunction (ED). An integrated analysis of five double-blind, placebo-controlled trials (N = 1 046) was performed. Patients were randomly assigned to receive 10 mg tadalafil (N = 185), 20 mg tadalafil (N = 510), or placebo (N = 351). Efficacy assessments included the International Index of Erectile Function (IIEF), Sexual Encounter Profile (SEP) diary and Global Assessment Question (GAQ). Patients receiving 10 mg or 20 mg tadalafil showed significant improvement from baseline-to-end point on the Erectile Function domain of the International Index of Erectile Function (IIEF-EF) domain score in all clinical sub-populations analyzed, compared with patients receiving placebo (P < 0.001). The 10-mg and 20-mg tadalafil groups showed a mean success rate of 64.1% and 70.5% for sexual intercourse attempts (SEP3, successful intercourse), respectively, compared with 33.4% in the placebo group (P < 0.001), and 85.5% and 85.4% reported improved erections at end point GAQ, respectively, versus 43.5% in the placebo group (P < 0.001). Tadalafil was well tolerated across all groups studied. Headache and back pain were the most frequently reported adverse events. Overall, tadalafil was effective and well tolerated across a diverse clinical spectrum of Asian men with ED.
我们评估了按需服用他达拉非在患有勃起功能障碍(ED)的亚洲男性这一多样化临床群体(患者人口统计学特征、疾病严重程度和合并症各不相同)中的疗效和安全性。我们对五项双盲、安慰剂对照试验(N = 1046)进行了综合分析。患者被随机分配接受10毫克他达拉非(N = 185)、20毫克他达拉非(N = 510)或安慰剂(N = 351)。疗效评估包括国际勃起功能指数(IIEF)、性经历记录(SEP)日记和总体评估问题(GAQ)。与接受安慰剂的患者相比,接受10毫克或20毫克他达拉非的患者在所有分析的临床亚组中,国际勃起功能指数(IIEF)的勃起功能领域评分从基线到终点均有显著改善(P < 0.001)。10毫克和20毫克他达拉非组性交尝试(SEP3,性交成功)的平均成功率分别为64.1%和70.5%,而安慰剂组为33.4%(P < 0.001),在终点GAQ中,分别有85.5%和85.4%的患者报告勃起改善,而安慰剂组为43.5%(P < 0.001)。在所研究的所有组中,他达拉非耐受性良好。头痛和背痛是最常报告的不良事件。总体而言,他达拉非在患有ED的亚洲男性的各种临床情况下均有效且耐受性良好。