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首页> 外文期刊>The journal of sexual medicine >Efficacy and safety of dapoxetine in men with premature ejaculation and concomitant erectile dysfunction treated with a phosphodiesterase type 5 inhibitor: Randomized, placebo-controlled, phase III study
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Efficacy and safety of dapoxetine in men with premature ejaculation and concomitant erectile dysfunction treated with a phosphodiesterase type 5 inhibitor: Randomized, placebo-controlled, phase III study

机译:达泊西汀对5型磷酸二酯酶抑制剂治疗的早泄及伴有勃起功能障碍的男性的疗效和安全性:随机,安慰剂对照,III期研究

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摘要

Introduction: Men with comorbid erectile dysfunction (ED) and premature ejaculation (PE) may be concomitantly prescribed a phosphodiesterase type 5 (PDE5) inhibitor and dapoxetine. Aim: Evaluate efficacy and safety of dapoxetine 30mg and 60mg on demand (prn) in men with PE and ED who were being treated with PDE5 inhibitors. Methods: This randomized, double-blind, placebo-controlled, flexible-dose, multicenter study enrolled men ≥18 years who met diagnostic criteria for PE including intravaginal ejaculatory latency time (IELT) of ≤2 minutes in ≥75% of sexual intercourse episodes; were on stable regimen of a PDE5 inhibitor; and had International Index of Erectile Function-erectile function domain score ≥21. Subjects received placebo, dapoxetine 30mg, or dapoxetine 60mg prn (1-3 hours before intercourse) for 12 weeks. Main Outcome Measure: Stopwatch-measured average IELT, Clinical Global Impression of Change (CGIC) in PE, Premature Ejaculation Profile (PEP), and treatment-emergent adverse events (TEAEs). Results: Of 495 subjects randomized, 429 completed the study. Arithmetic mean average IELT significantly increased with dapoxetine vs. placebo at end point (5.2 vs. 3.4 minutes) and weeks 4, 8, and 12 (P≤0.002 for all). Men who described their PE at least "better" using the CGIC were significantly greater with dapoxetine vs. placebo at end point (56.5% vs. 35.4%) and weeks 4, 8, and 12 (P≤0.001 for all). Significantly better outcomes were also reported with dapoxetine vs. placebo on PEP measures. Incidence of TEAEs was 20.0% and 29.6% in placebo- and dapoxetine-treated subjects, respectively (P=0.0135). TEAEs led to discontinuation in 1.6% of subjects in both groups. Most frequent TEAEs were known adverse drug reactions of dapoxetine treatment including nausea (9.2%), headache (4.4%), diarrhea (3.6%), dizziness (2.4%), and dizziness postural (2.4%). Conclusions: In men with PE and comorbid ED on a stable regimen of PDE5 inhibitor, dapoxetine provided meaningful treatment benefit and was generally well tolerated. McMahon CG, Giuliano F, Dean J, Hellstrom WJG, Bull S, Tesfaye F, Sharma O, Rivas DA, and Aquilina JW. Efficacy and safety of dapoxetine in men with premature ejaculation and concomitant erectile dysfunction treated with a phosphodiesterase type 5 inhibitor: Randomized, placebo-controlled, phase III study. J Sex Med 2013;10:2312-2325.
机译:简介:合并勃起功能障碍(ED)和早泄(PE)的男性可能同时服用5型磷酸二酯酶(PDE5)抑制剂和达泊西汀。目的:评估在接受PDE5抑制剂治疗的PE和ED男性中按需剂量(prn)达泊西汀30mg和60mg的疗效和安全性。方法:这项随机,双盲,安慰剂对照,灵活剂量,多中心研究纳入了≥18岁且符合PE诊断标准的男性,其中包括≥75%的性交发作中阴道内射精潜伏时间(IELT)≤2分钟;采用稳定的PDE5抑制剂治疗方案;且勃起功能国际指数-勃起功能域得分≥21。受试者接受安慰剂,达泊西汀30mg或达泊西汀60mg prn(性交前1-3小时)治疗12周。主要观察指标:秒表测量的平均IELT,PE的临床总体变化印象(CGIC),早泄概况(PEP)和治疗紧急不良事件(TEAE)。结果:在495名随机受试者中,有429名完成了研究。在终点(5.2 vs. 3.4分钟)以及第4、8和12周时,达泊西汀与安慰剂的算术平均IELT显着增加。使用CGIC描述其PE至少“更好”的男性,在终点时达泊西汀与安慰剂的比例分别为56.5%与35.4%,显着更高(第4、8和12周,所有P均≤0.001)。达泊西汀与安慰剂相比,PEP措施的结果也有明显改善。在接受安慰剂和达泊西汀治疗的受试者中,TEAE的发生率分别为20.0%和29.6%(P = 0.0135)。 TEAEs导致两组中有1.6%的受试者停药。已知最常见的TEAE是达泊西汀治疗的不良药物反应,包括恶心(9.2%),头痛(4.4%),腹泻(3.6%),头晕(2.4%)和头晕姿势(2.4%)。结论:对于患有PE和ED并存的PDE5抑制剂稳定方案的男性,达泊西汀提供了有意义的治疗益处,并且总体上具有良好的耐受性。麦克马洪(McMahon)CG,朱利亚诺(Giuliano F),迪安(Jean),赫尔斯特罗姆(Hellstrom)WJG,公牛S,特斯法耶(Tesfaye)F,沙玛(Sharma)O,里瓦斯(Rivas DA)和阿奎琳娜(Aquilina)达泊西汀对男性早泄并伴有勃起功能障碍的男性进行磷酸二酯酶5型抑制剂治疗的疗效和安全性:随机,安慰剂对照的III期研究。 J Sex Med 2013; 10:2312-2325。

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