首页> 外文期刊>International journal of clinical practice >A 6-month study of the efficacy and safety of tadalafil in the treatment of erectile dysfunction: a randomised, double-blind, parallel-group, placebo-controlled study in Australian men.
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A 6-month study of the efficacy and safety of tadalafil in the treatment of erectile dysfunction: a randomised, double-blind, parallel-group, placebo-controlled study in Australian men.

机译:他达拉非治疗勃起功能障碍的功效和安全性的为期6个月的研究:一项针对澳大利亚男性的随机,双盲,平行组,安慰剂对照研究。

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摘要

The efficacy and safety of tadalafil for the treatment of erectile dysfunction (ED) were assessed in a 6-month, randomised, double-blind, placebo-controlled study. Australian men with mild, moderate or severe ED of organic, psychogenic or mixed aetiology were randomised to tadalafil 20 mg as needed (n = 93) or placebo (n = 47). Efficacy assessments included the international index of erectile function (IIEF) and the sexual encounter profile (SEP) diary. Tadalafil significantly improved erectile function compared with placebo (p < 0.001, all measures). At the end of the study, the mean per-patient proportion of successful sexual intercourse attempts (SEP question three) was 73.5% for patients treated with tadalafil and 26.8% for placebo-treated patients. Improved erections were reported by 78% of tadalafil-treated patients compared to 12.8% of placebo-treated patients. The most common treatment-emergent adverse events--headache and dyspepsia--were generally mild or moderate. Tadalafil was effective and well tolerated in Australian men with mild to severe ED.
机译:在一个为期6个月的随机,双盲,安慰剂对照研究中,评估了他达拉非治疗勃起功能障碍(ED)的疗效和安全性。根据需要,将患有有机,精神病或混合病因的轻度,中度或重度ED的澳大利亚男性随机分为他达拉非20 mg(n = 93)或安慰剂(n = 47)。效能评估包括国际勃起功能指数(IIEF)和性遭遇概况(SEP)日记。与安慰剂相比,他达拉非显着改善了勃起功能(p <0.001,所有指标)。在研究结束时,他达拉非治疗的患者成功性交尝试的平均每名患者比例(SEP问题三)为73.5%,安慰剂治疗的患者为26.8%。据报道,接受他达拉非治疗的患者的勃起得到改善,为78%,而接受安慰剂治疗的患者为12.8%。最常见的紧急治疗不良事件-头痛和消化不良-一般为轻度或中度。他达拉非对轻度至重度ED的澳大利亚男性有效且耐受良好。

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