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首页> 外文期刊>Mayo Clinic Proceedings >Sustained efficacy and safety of vardenafil for treatment of erectile dysfunction: a randomized, double-blind, placebo-controlled study.
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Sustained efficacy and safety of vardenafil for treatment of erectile dysfunction: a randomized, double-blind, placebo-controlled study.

机译:伐地那非治疗勃起功能障碍的持续疗效和安全性:一项随机,双盲,安慰剂对照研究。

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摘要

OBJECTIVE: To evaluate the reliability, efficacy, and safety of vardenafil, 10 mg, for patients with erectile dysfunction. PATIENTS AND METHODS: Vardenafil-naive patients completed a 4-week treatment-free run-in phase and a 1-week single-dose vardenafil (10 mg) open-label challenge phase. Responders to vardenafil in the challenge phase were randomized to 12 weeks of double-blind, fixed-dose treatment with vardenafil at 10 mg or placebo. Diary responses to Sexual Encounter Profile (SEP) questions about erections and attempts at sexual activity were collected after 4, 8, and 12 weeks of randomized treatment. Adverse events were monitored throughout the study. RESULTS: During the open-label challenge phase, the proportions of patients with a first-time success for penetration (SEP2) and maintenance of erection (SEP3) were 87% and 74%, respectively. Of 600 patients challenged with a single dose of vardenafil at 10 mg, 260 were randomized to vardenafil and 263 to placebo. During the double-blind phase, the reliability of penetration and maintenance rates for patients successful during the challenge phase were significantly greater with vardenafil compared with placebo (83.4% vs 55.8% [SEP2] and 76.6% vs 42.1% [SEP3], respectively). At week 12, patients in the vardenafil group had a consistently higher least squares mean (SE) on the erectile function domain score of the International Index of Erectile Function than patients in the placebo group (23.5 [0.4] vs 15.8 [0.4], respectively [last observation carried forward]) and a greater proportion of positive responses to the Global Assessment Question (80.8% vs 32.3%, respectively [last observation carried forward]) at each assessment (Pc.001). Vardenafil was generally well tolerated; most adverse events were mild to moderate, with headache and flushing reported most frequently. CONCLUSION: During this 12-week study, vardenafil produced consistently higher reliability of penetration and maintenance of erection rates compared to placebo and was generally well tolerated in patients with erectile dysfunction.
机译:目的:评价伐地那非10 mg对勃起功能障碍患者的可靠性,疗效和安全性。患者和方法:初用伐地那非的患者完成了为期4周的无治疗磨合期和为期1周的单剂量伐地那非(10 mg)开放标签激发期。攻击期对伐地那非的反应者被随机分为12周的双盲,固定剂量的10毫克伐地那非或安慰剂治疗。在随机治疗的第4、8和12周后,收集了有关性生活经历(SEP)有关勃起和性活动尝试的日记的答案。在整个研究过程中监测不良事件。结果:在开放标签挑战阶段,首次成功穿透(SEP2)和维持勃起(SEP3)的患者比例分别为87%和74%。在600名接受单剂量伐地那非10 mg攻击的患者中,有260名被随机分配给伐地那非,263名被随机分配给安慰剂。在双盲阶段,使用伐地那非的患者在攻击阶段成功穿透和维持率的可靠性显着高于安慰剂(分别为83.4%vs 55.8%[SEP2]和76.6%vs 42.1%[SEP3]) 。在第12周时,伐地那非组的患者在国际勃起功能指数的勃起功能域评分上的最低平方均值(SE)始终高于安慰剂组(分别为23.5 [0.4]和15.8 [0.4]) [最后的观察结果])和每次评估时对全球评估问题的正面回答比例(分别为80.8%和32.3%[最后的观察结果])(Pc.001)。伐地那非的耐受性良好。大多数不良事件为轻度至中度,头痛和潮红最常见。结论:在这项为期12周的研究中,伐地那非与安慰剂相比,始终具有较高的渗透可靠性和勃起速率,并且在勃起功能障碍患者中一般耐受良好。

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