Chiang H S, Hwang T I S, Hsui Y S, Lin Y C, Chen H E, Chen G C, Liao C H
Division of Urology, Department of Surgery, Shin Kong WHS Memorial Hospital, Taipei, Taiwan, ROC.
Int J Impot Res. 2007 Jul-Aug;19(4):411-7. doi: 10.1038/sj.ijir.3901562. Epub 2007 May 31.
A randomized, double-blind, placebo-controlled trial was conducted to (1) evaluate efficacy and safety of transdermal testosterone gel (AndroGel) for hypogonadal men in Taiwan, and (2) observe improvements in sexual function through international index of erectile function (IIEF) scores. Eligible hypogonadal men were randomized to receive 50 mg/day transdermal testosterone gel (TTG) or placebo for 3 months. Primary end point was change from baseline in total testosterone (TT) and free testosterone (FT). Secondary end points were change from baseline in serum hormone levels (such as dihydrotestosterone (DHT), estradiol (E2), luteinizing hormone (LH), follicle-stimulating hormone (FSH) and sex-hormone-binding globulin (SHBG)) and changes in IIEF scores. Safety evaluations included adverse events (AEs) and skin irritation assessment. Compared with baseline, the TTG group (n=20) had statistically significant increases in mean TT levels at month 1 (P=0.024) and month 2 (P=0.025), but no significant changes at month 3. TT levels in the placebo group (n=18) showed no statistically significant change at any visit. Changes in FT levels paralleled changes in TT levels in both groups. TTG group IIEF scores were significantly increased at month 3 (P=0.01), compared with a decline in placebo scores. No drug-related AEs occurred in the TTG group; the placebo group had 2 AEs (mild skin rash). In conclusion, TTG effectively restores serum TT and FT levels to a normal physiological range for hypogonadal men in Taiwan and improves sexual function.
进行了一项随机、双盲、安慰剂对照试验,以(1)评估透皮睾酮凝胶(安特尔)对台湾性腺功能减退男性的疗效和安全性,以及(2)通过国际勃起功能指数(IIEF)评分观察性功能的改善情况。符合条件的性腺功能减退男性被随机分为接受50毫克/天的透皮睾酮凝胶(TTG)或安慰剂治疗3个月。主要终点是总睾酮(TT)和游离睾酮(FT)相对于基线的变化。次要终点是血清激素水平(如双氢睾酮(DHT)、雌二醇(E2)、黄体生成素(LH)、卵泡刺激素(FSH)和性激素结合球蛋白(SHBG))相对于基线的变化以及IIEF评分的变化。安全性评估包括不良事件(AE)和皮肤刺激评估。与基线相比,TTG组(n = 20)在第1个月(P = 0.024)和第2个月(P = 0.025)时平均TT水平有统计学显著升高,但在第3个月时无显著变化。安慰剂组(n = 18)的TT水平在任何一次访视时均无统计学显著变化。两组中FT水平的变化与TT水平的变化平行。TTG组在第3个月时IIEF评分显著升高(P = 0.01),而安慰剂组评分下降。TTG组未发生与药物相关的不良事件;安慰剂组有2例不良事件(轻度皮疹)。总之,TTG能有效将台湾性腺功能减退男性的血清TT和FT水平恢复到正常生理范围并改善性功能。