首页> 外文期刊>The journal of sexual medicine >Efficacy of udenafil for the treatment of erectile dysfunction up to 12 hours after dosing: a randomized placebo-controlled trial.
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Efficacy of udenafil for the treatment of erectile dysfunction up to 12 hours after dosing: a randomized placebo-controlled trial.

机译:给药后12小时内,乌地那非治疗勃起功能障碍的功效:一项随机安慰剂对照试验。

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INTRODUCTION: Udenafil is a newly developed selective phosphodiesterase type 5 inhibitor for the treatment of men with erectile dysfunction (ED). AIM: To evaluate the efficacy of udenafil in treating ED for up to 12 hours after dosing. METHODS: This was a randomized, double-blind, placebo-controlled, parallel-group, fixed dose design, multicenter study. Following a 4-week nondrug baseline period, 104 men with ED of broad etiology and severity were randomized to one of two treatment groups: udenafil 100 mg or placebo. Participants were requested to attempt sexual intercourse at 12 hours after udenafil or placebo dosing during a 4-week treatment period. MAIN OUTCOME MEASURES: The primary efficacy variable was the response of patients to question 3 of the Sexual Encounter Profile (SEP Q3). The secondary efficacy measures were the response of patients to question 2 of the Sexual Encounter Profile (SEP Q2). Additional secondary efficacy measures included changes from baseline in the erectile function (EF) domain scores of the International Index of Erectile Function (IIEF) questionnaire. RESULTS: Of the 104 patients, 103 (50 in the udenafil group, 53 in the placebo group) completed the study. Udenafil significantly enhanced the rate of maintenance of erection (SEP Q3; placebo, 28.3% vs. udenafil, 54.7%; P < 0.0001). Significant change from baseline in the IIEF-EF domain was observed in the udenafil group (placebo, -0.58 +/- 0.67; udenafil, 4.40 +/- 0.84; P < 0.0001). For SEP Q2, there was no difference from baseline and no difference between the two groups. The overall adverse events rate was 11.3%. Most adverse events were mild or moderate in severity, and no serious adverse events were reported during the study and the follow-up period. CONCLUSIONS: Udenafil at 100 mg was effective for relieving ED for up to 12 hours after dosing. This duration of effectiveness could allow for flexibility and spontaneity in the sexual lives of patients.
机译:简介:乌地那非是一种新开发的选择性磷酸二酯酶5型抑制剂,用于治疗勃起功能障碍(ED)的男性。目的:评估给药后长达12小时的udenafil治疗ED的疗效。方法:这是一项随机,双盲,安慰剂对照,平行组,固定剂量设计,多中心研究。在为期4周的非药物基线期后,将104例病因和病情严重的ED男性随机分为两个治疗组之一:udenafil 100 mg或安慰剂。在4周的治疗期内,要求参与者在服用udenafil或安慰剂后12小时尝试性交。主要观察指标:主要疗效变量是患者对性接触情景(SEP Q3)问题3的反应。次要疗效指标是患者对“性相遇记录”(SEP Q2)问题2的反应。其他辅助功效指标包括国际勃起功能指数(IIEF)问卷中勃起功能(EF)域得分的基线变化。结果:在104位患者中,有103位(乌地那非组50位,安慰剂组53位)完成了研究。乌地那非显着提高了勃起维持率(SEP Q3;安慰剂28.3%,而乌地那非54.7%; P <0.0001)。在乌地那非组中观察到IIEF-EF域的基线有明显变化(安慰剂,-0.58 +/- 0.67;乌地那非,4.40 +/- 0.84; P <0.0001)。对于SEP Q2,与基线无差异,两组之间也无差异。总体不良事件发生率为11.3%。大多数不良事件的严重程度为轻度或中度,在研究和随访期间未报告严重不良事件。结论:100毫克的Udenafil可以在给药后长达12小时内有效缓解ED。有效期的持续时间可以允许患者性生活中的灵活性和自发性。

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