Testosterone patch increases sexual activity and desire in surgically menopausal women with hypoactive sexual desire disorder

被引:316
|
作者
Simon, J
Braunstein, G
Nachtigall, L
Utian, W
Katz, M
Miller, S
Waldbaum, A
Bouchard, C
Derzko, C
Buch, A
Rodenberg, C
Lucas, J
Davis, S
机构
[1] Womens Hlth Res Ctr, Laurel, MD 20707 USA
[2] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[3] NYU, Sch Med, New York, NY 10016 USA
[4] Rapid Med Res, Cleveland, OH 44122 USA
[5] Katz Kade & Hewitt Inc, Cincinnati, OH 45219 USA
[6] SAM Clin Res Ctr, San Antonio, TX 78229 USA
[7] Downtown Womens Hlth Care, Denver, CO 80202 USA
[8] Clin RSF Inc, Quebec City, PQ G1S 2L6, Canada
[9] St Michaels Hosp, Ctr Hlth, Toronto, ON M5B 1W8, Canada
[10] Procter & Gamble Pharmaceut Hlth Care Res Ctr, Mason, OH 45040 USA
[11] Jean Hailes Fdn, Res Unit, Clayton, Vic 3168, Australia
[12] Monash Univ, Dept Med, Praham, Vic 3800, Australia
来源
关键词
D O I
10.1210/jc.2004-1747
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: 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. Objective: The objective of this study was to evaluate the efficacy and safety of a testosterone patch in surgically menopausal women with HSDD. Design: The design was a randomized, double-blind, parallel-group, placebo-controlled, 24-wk study (the Intimate SM 1 study). Setting: The study was performed at private or institutional practices. Patients: 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 mu g/d (n = 283) was administered. There were 19 patients who withdrew due to adverse events in the placebo group and 24 in the 300 mu g/d testosterone group. Intervention: Testosterone (300 mu g/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. Results: 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. Conclusion: 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.
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页码:5226 / 5233
页数:8
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