Suppr超能文献

一项多中心、随机、双盲、交叉研究,旨在探讨勃起功能障碍治疗起始阶段患者对20毫克他达拉非或50毫克枸橼酸西地那非的偏好。

A multicenter, randomized, double-blind, crossover study of patient preference for tadalafil 20 mg or sildenafil citrate 50 mg during initiation of treatment for erectile dysfunction.

作者信息

Govier Fred, Potempa Axel-Juerg, Kaufman Joel, Denne Jonathan, Kovalenko Pavel, Ahuja Sanjeev

机构信息

Department of Urology, Virginia Mason Medical Center, Seattle, Washington 98111, USA.

出版信息

Clin Ther. 2003 Nov;25(11):2709-23. doi: 10.1016/s0149-2918(03)80328-4.

Abstract

BACKGROUND

Tadalafil is a phosphodiesterase 5 (PDE5) inhibitor approved in >30 countries for the treatment of erectile dysfunction (ED). It has been shown to improve erectile function compared with placebo in Phase III studies, but clinical experience comparing tadalafil with the PDE5 inhibitor sildenafil citrate is lacking.

OBJECTIVE

This study compared patient preference for tadalafil 20 mg or sildenafil 50 mg during initial treatment for ED. It also compared the tolerability of the 2 agents at these doses.

METHODS

This randomized, double-blind, fixed-dose, 2-period crossover trial took place at 13 sites in the United States and Germany. Patients were randomized 1:1 to receive 4 weeks of treatment with tadalafil 20 mg or sildenafil 50 mg, followed by the alternative treatment, to be taken as needed up to once daily before sexual activity.

RESULTS

The study enrolled 215 men with ED, 109 randomized to the tadalafil-sildenafil sequence and 106 to the sildenafil-tadalafil sequence. Their mean age was 49.8 years; 84.7% were sildenafil naive and 15.3% had undergone a previous inadequate trial of sildenafil. Most patients had moderate ED (60.5%) of >or=1 year's duration (74.9%). Of 190 evaluable patients, 126 (66.3%) preferred to initiate treatment with tadalafil, compared with 64 (33.7%) with sildenafil (P < 0.001). Patients' preference did not differ by age, duration of ED, treatment sequence, or previous sildenafil exposure. Both medications were well tolerated, with no significant differences in the incidence of treatment-emergent adverse events. Headache (11.2% tadalafil, 8.8% sildenafil), dyspepsia (6.0% and 4.2%, respectively), nasopharyngitis (4.7% and 2.8%), and flushing (2.8% and 4.7%) were the most common adverse events. The rate of ocular disturbances was low: 1 patient experienced intermittent bilateral reduction in visual acuity with tadalafil, and 2 exhibited conjunctival hyperemia or eyelid edema with sildenafil.

CONCLUSIONS

Tadalafil 20 mg was preferred to sildenafil 50 mg for the initiation of ED therapy in this study population. Both medications were well tolerated.

摘要

背景

他达拉非是一种磷酸二酯酶5(PDE5)抑制剂,已在30多个国家获批用于治疗勃起功能障碍(ED)。在III期研究中,与安慰剂相比,它已被证明可改善勃起功能,但缺乏他达拉非与PDE5抑制剂枸橼酸西地那非对比的临床经验。

目的

本研究比较了在ED初始治疗期间患者对20mg他达拉非或50mg西地那非的偏好。还比较了这两种药物在这些剂量下的耐受性。

方法

这项随机、双盲、固定剂量、两阶段交叉试验在美国和德国的13个地点进行。患者按1:1随机分组,接受4周的20mg他达拉非或50mg西地那非治疗,随后接受替代治疗,按需在性活动前每日服用一次。

结果

该研究纳入了215名ED男性,109名随机接受他达拉非-西地那非治疗顺序,106名接受西地那非-他达拉非治疗顺序。他们的平均年龄为49.8岁;84.7%既往未使用过西地那非,15.3%曾有过西地那非治疗效果不佳的经历。大多数患者患有中度ED(60.5%),病程≥1年(74.9%)。在190名可评估患者中,126名(66.3%)更倾向于开始使用他达拉非治疗,而64名(33.7%)更倾向于使用西地那非(P<0.001)。患者的偏好不受年龄、ED病程、治疗顺序或既往西地那非使用情况的影响。两种药物耐受性均良好,治疗中出现的不良事件发生率无显著差异。头痛(他达拉非组为11.2%,西地那非组为8.8%)、消化不良(分别为6.0%和4.2%)、鼻咽炎(分别为4.7%和2.8%)和潮红(分别为2.8%和4.7%)是最常见的不良事件。眼部不适发生率较低:1名患者使用他达拉非后出现间歇性双侧视力下降,2名患者使用西地那非后出现结膜充血或眼睑水肿。

结论

在本研究人群中,ED治疗起始时,20mg他达拉非比50mg西地那非更受青睐。两种药物耐受性均良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验