Department of Urology, Seoul National University Hospital, Seoul, Korea.
J Sex Med. 2010 Sep;7(9):3143-52. doi: 10.1111/j.1743-6109.2010.01926.x.
Mirodenafil is a recently developed oral phosphodiesterase type 5 inhibitor, which was observed to significantly improve erectile function and was well tolerated in men with broad-spectrum erectile dysfunction (ED).
To investigate the efficacy and safety of mirodenafil treatment compared with placebo in men taking at least one antihypertensive medication.
A multicenter, double-blind, placebo-controlled, parallel group, fixed-dose study was conducted with 109 subjects who were randomized to placebo or mirodenafil 100 mg for 12 weeks on an "as needed" basis.
The primary efficacy measures were the changes from baseline in sum of scores on International Index of Erectile Function-erectile function domain (IIEF-EF) questions 1 to 5 and 15 with treatment. The secondary efficacy measures included scores on IIEF question 3 and 4 (Q3 and Q4), all domain scores of IIEF, and Sexual Encounter Profile Question 2 and 3 (SEP2 and SEP3) along with responses to Global Assessment Question (GAQ) and Life Satisfaction Checklist (LSC). The safety assessments included laboratory tests, vital signs, 12-lead electrocardiogram recordings, and patients' reporting of adverse events.
The mirodenafil group showed significantly greater increase in IIEF-EF scores at 12 weeks compared with the placebo group (9.35 ± 6.86 vs. 2.66 ± 6.44, P<0.001). The mirodenafil group also demonstrated significantly greater improvement in scores of IIEF Q3 and Q4, other four domains of IIEF, SEP2, SEP3, and LSC along with percentages of patients responding positively to GAQ compared with the placebo group. During the study, no clinically significant changes were observed regarding blood pressure, heart rate, electrocardiographic findings, or laboratory values. Facial flushing and headache were the most common treatment-associated adverse events, which were mild or moderate in severity, resolving spontaneously.
Mirodenafil was effective and safe in men with ED concomitantly taking antihypertensive medications.
米罗地尔是一种新开发的口服磷酸二酯酶 5 抑制剂,在治疗广谱勃起功能障碍(ED)患者时,观察到其能显著改善勃起功能且具有良好的耐受性。
研究米罗地尔治疗与安慰剂在同时服用至少一种降压药物的男性中的疗效和安全性。
进行了一项多中心、双盲、安慰剂对照、平行组、固定剂量研究,共纳入 109 名受试者,他们被随机分配至安慰剂或米罗地尔 100mg 组,按需治疗 12 周。
主要疗效测量指标为治疗后国际勃起功能指数-勃起功能域(IIEF-EF)问题 1 至 5 及 15 的总分变化。次要疗效测量指标包括 IIEF 问题 3 和 4(Q3 和 Q4)、IIEF 所有域评分、性遭遇剖面图问题 2 和 3(SEP2 和 SEP3)以及全球评估问题(GAQ)和生活满意度检查表(LSC)的应答情况。安全性评估包括实验室检查、生命体征、12 导联心电图记录以及患者报告的不良事件。
与安慰剂组相比,米罗地尔组在 12 周时 IIEF-EF 评分显著增加(9.35±6.86 对 2.66±6.44,P<0.001)。米罗地尔组在 IIEF Q3 和 Q4、IIEF 其他四个域、SEP2、SEP3 和 LSC 的评分以及对 GAQ 做出阳性应答的患者比例方面也表现出显著的改善,与安慰剂组相比,这些方面均有统计学意义。研究期间,血压、心率、心电图发现或实验室值均无临床意义的变化。面部潮红和头痛是最常见的治疗相关不良事件,其严重程度为轻度或中度,且可自行缓解。
米罗地尔对同时服用降压药物的 ED 男性有效且安全。