Simon James, Braunstein Glenn, Nachtigall Lila, Utian Wulf, Katz Molly, Miller Sam, Waldbaum Arthur, Bouchard Celine, Derzko Christine, Buch Akshay, Rodenberg Cynthia, Lucas Johna, Davis Susan
Women's Health Research Center (J.S.), Laurel, Maryland 20707, USA.
J Clin Endocrinol Metab. 2005 Sep;90(9):5226-33. doi: 10.1210/jc.2004-1747. Epub 2005 Jul 12.
Hypoactive sexual desire disorder (HSDD) is one of the most common sexual problems reported by women, but few studies have been conducted to evaluate treatments for this condition.
The objective of this study was to evaluate the efficacy and safety of a testosterone patch in surgically menopausal women with HSDD.
The design was a randomized, double-blind, parallel-group, placebo-controlled, 24-wk study (the Intimate SM 1 study).
The study was performed at private or institutional practices.
The subjects studied were women, aged 26-70 yr, with HSDD after bilateral salpingo-oophorectomy who were receiving concomitant estrogen therapy. Placebo (n = 279) or testosterone 300 microg/d (n = 283) was administered. There were 19 patients who withdrew due to adverse events in the placebo group and 24 in the 300 mug/d testosterone group.
Testosterone (300 microg/d) or placebo patches were applied twice weekly.
MAIN OUTCOME MEASURE(S): The primary end point was the change in the frequency of total satisfying sexual activity at 24 wk. Secondary end points included other sexual functioning end points and safety assessments.
At 24 wk, there was an increase from baseline in the frequency of total satisfying sexual activity of 2.10 episodes/4 wk in the testosterone group, which was significantly greater than the change of 0.98 episodes/4 wk in the placebo group (P = 0.0003). The testosterone group also experienced statistically significant improvements in sexual desire and a decrease in distress. The overall safety profile was similar in both treatment groups.
In the Intimate SM 1 study, the testosterone patch improved sexual function and decreased distress in surgically menopausal women with HSDD and was well tolerated in this trial.
性欲减退障碍(HSDD)是女性报告的最常见的性问题之一,但针对该病症治疗方法的评估研究较少。
本研究旨在评估睾酮贴片治疗手术绝经后患有HSDD女性的疗效和安全性。
该研究为随机、双盲、平行组、安慰剂对照的24周研究(亲密SM 1研究)。
研究在私人或机构诊所进行。
研究对象为年龄在26 - 70岁之间、双侧输卵管卵巢切除术后患有HSDD且正在接受雌激素替代治疗的女性。给予安慰剂(n = 279)或300微克/天睾酮(n = 283)治疗。安慰剂组有19例患者因不良事件退出,300微克/天睾酮组有24例。
每周两次应用睾酮(300微克/天)或安慰剂贴片。
主要终点是24周时总满意性活动频率的变化。次要终点包括其他性功能终点和安全性评估。
24周时,睾酮组总满意性活动频率较基线增加2.10次/4周,显著高于安慰剂组的0.98次/4周(P = 0.0003)。睾酮组在性欲方面也有统计学意义上的显著改善,痛苦感降低。两个治疗组的总体安全性相似。
在亲密SM 1研究中,睾酮贴片改善了手术绝经后患有HSDD女性的性功能并减轻了痛苦感,且在该试验中耐受性良好。