Department of Urology, Seoul National University Hospital, 28, Yongon-dong, Chongno-gu, Seoul, 110-744, Korea.
J Sex Med. 2009 Nov;6(11):3166-76. doi: 10.1111/j.1743-6109.2009.01456.x. Epub 2009 Aug 17.
Erectile dysfunction (ED) and hypertension are frequent comorbid conditions. The vasodilating properties of type 5 phosphodiesterase inhibitor (PDE5I) are the major concerns for the treatment of ED patients on antihypertensive medications.
To evaluate the efficacy and safety of Udenafil [Zydena] (Dong-A, Seoul, Korea), a newly developed PDE5I, for the treatment of ED patients on antihypertensive medication.
It was a multicentered, randomized, double-blind, placebo-controlled, fix-dosed clinical trial among 165 ED patients receiving antihypertensive medications. The subjects treated with placebo, 100 mg or 200 mg of Udenafil for 12 weeks were asked to complete the Sexual Encounter Profile (SEP) diary, the International Index of Erectile Function (IIEF), and the Global Assessment Question (GAQ) during the study period.
Primary parameter: the change from baseline for IIEF erectile function domain (EFD) score; Secondary parameters: the IIEF Question 3 and 4, SEP Question 2 and 3, the rate of achieving normal erectile function (EFD > or = 26) and the response to GAQ.
Compared to placebo, patients receiving both doses of Udenafil showed significantly improved the IIEF-EFD score. The least squares means for the change from baseline in IIEF-EFD scores were 8.4 and 9.8 for 100 mg and 200 mg Udenafil groups, respectively; those values were significantly higher than that of placebo (2.4, P < 0.0001). Similar results were observed in the comparison of Q3 and Q4 of IIEF, SEP diary and GAQ. Headache and flushing were the most common treatment-emergent adverse events, which were transient and mild-to-moderate in nature. No parameters of efficacy and safety were affected among the subsets stratified according to either the number of antihypertensive medication received or the previous experience of PDE5Is treatment.
Udenafil significantly improved erectile function among ED patients with hypertensive symptom treated with concomitant antihypertensive medication. The treatment did not increase the frequency or severity of adverse events.
勃起功能障碍(ED)和高血压是常见的合并症。5 型磷酸二酯酶抑制剂(PDE5I)的血管舒张特性是治疗正在服用抗高血压药物的 ED 患者的主要关注点。
评估新开发的 PDE5I 乌地那非(Dong-A,首尔,韩国)治疗正在服用抗高血压药物的 ED 患者的疗效和安全性。
这是一项在 165 名接受抗高血压药物治疗的 ED 患者中进行的多中心、随机、双盲、安慰剂对照、固定剂量的临床试验。接受安慰剂、100mg 或 200mg 乌地那非治疗 12 周的患者在研究期间完成了性经历问卷(SEP)日记、国际勃起功能指数(IIEF)和全球评估问题(GAQ)。
主要参数:IIEF 勃起功能域(EFD)评分的基线变化;次要参数:IIEF 问题 3 和 4、SEP 问题 2 和 3、实现正常勃起功能(EFD≥26)的比例和对 GAQ 的反应。
与安慰剂相比,接受乌地那非治疗的患者 IIEF-EFD 评分显著改善。乌地那非 100mg 和 200mg 组 IIEF-EFD 评分的基线变化最小平方均值分别为 8.4 和 9.8;与安慰剂相比,这些值显著升高(2.4,P<0.0001)。在 IIEF 的 Q3 和 Q4、SEP 日记和 GAQ 的比较中也观察到了类似的结果。头痛和潮红是最常见的治疗后不良事件,性质为一过性和轻中度。根据接受的抗高血压药物数量或之前 PDE5I 治疗的经验对亚组进行分层,疗效和安全性参数不受影响。
乌地那非可显著改善正在接受抗高血压药物治疗的高血压症状 ED 患者的勃起功能。治疗并未增加不良事件的频率或严重程度。