San Diego Sexual Medicine, Alvarado Hospital, CA 92120, USA.
Mayo Clin Proc. 2012 Sep;87(9):843-52. doi: 10.1016/j.mayocp.2012.06.016. Epub 2012 Aug 1.
To prospectively assess the safety and effectiveness of the investigational phosphodiesterase 5 inhibitor avanafil to treat erectile dysfunction in men with diabetes mellitus.
This 12-week, multicenter, double-blind, placebo-controlled study conducted between December 15, 2008, and February 11, 2010, randomized 390 men with diabetes and erectile dysfunction 1:1:1 to receive avanafil, 100 mg (n=129), avanafil, 200 mg (n=131), or placebo (n=130). Coprimary end points assessed changes in the percentage of sexual attempts in which men were able to maintain an erection of sufficient duration to have successful intercourse (Sexual Encounter Profile [SEP] 3), percentage of sexual attempts in which men were able to insert the penis into the partner's vagina (SEP 2), and International Index of Erectile Function erectile function domain score.
Compared with placebo, least-squares mean change from baseline to study end in SEP 3, SEP 2, and International Index of Erectile Function erectile function domain score were significantly improved with both avanafil, 100 mg (P≤.002), and avanafil, 200 mg (P<.001). Additional analyses indicated that successful intercourse could be initiated in 15 minutes or less through more than 6 hours after avanafil dosing. Adverse events most commonly reported with avanafil treatment were headache, nasopharyngitis, flushing, and sinus congestion.
Avanafil was safe and effective for treating erectile dysfunction in men with diabetes and was effective as early as 15 minutes and more than 6 hours after dosing. The adverse events seen with avanafil were similar to those seen with other phosphodiesterase 5 inhibitors.
clinicaltrials.gov Identifier NCT00809471.
前瞻性评估磷酸二酯酶 5 抑制剂阿伐那非治疗糖尿病男性勃起功能障碍的安全性和有效性。
这项为期 12 周、多中心、双盲、安慰剂对照研究于 2008 年 12 月 15 日至 2010 年 2 月 11 日进行,将 390 名患有糖尿病和勃起功能障碍的男性随机分为 1:1:1 接受阿伐那非 100mg(n=129)、阿伐那非 200mg(n=131)或安慰剂(n=130)治疗。主要终点评估了男性能够维持足够勃起以进行成功性交的性尝试比例(性经历概况[SEP]3)、男性能够将阴茎插入伴侣阴道的性尝试比例(SEP2)和国际勃起功能指数勃起功能域评分的变化。
与安慰剂相比,阿伐那非 100mg(P≤.002)和阿伐那非 200mg(P<.001)治疗后,SE3、SE2 和国际勃起功能指数勃起功能域评分的基线至研究结束时的最小二乘均数变化均显著改善。进一步分析表明,阿伐那非给药后 15 分钟内或 6 小时后即可开始进行成功性交。阿伐那非治疗最常见的不良反应是头痛、鼻咽炎、潮红和鼻窦充血。
阿伐那非治疗糖尿病男性勃起功能障碍安全有效,起效时间早于给药后 15 分钟,可维持 6 小时以上。阿伐那非的不良反应与其他磷酸二酯酶 5 抑制剂相似。
clinicaltrials.gov 标识符 NCT00809471。