Testosterone Patch Increases Sexual Activity and Desire in Surgically Menopausal Women with Hypoactive Sexual Desire Disorder

Author:

Simon James1,Braunstein Glenn2,Nachtigall Lila3,Utian Wulf4,Katz Molly5,Miller Sam6,Waldbaum Arthur7,Bouchard Celine8,Derzko Christine9,Buch Akshay10,Rodenberg Cynthia10,Lucas Johna10,Davis Susan1112

Affiliation:

1. Women’s Health Research Center (J.S.), Laurel, Maryland 20707;

2. Cedars-Sinai Medical Center (G.B.), Los Angeles, California 90048;

3. New York University School of Medicine (L.N.), New York, New York 10016;

4. Rapid Medical Research (W.U.), Cleveland, Ohio 44122;

5. Katz, Kade, and Hewitt, Inc. (M.K.), Cincinnati, Ohio 45219;

6. S. A. M. Clinical Research Center (S.M.), San Antonio, Texas 78229;

7. Downtown Women’s Health Care (A.W.), Denver, Colorado 80202;

8. Clinique RSF, Inc. (C.B.), Quebec, Canada G1S 2L6;

9. St. Michael’s Hospital Health Center (C.D.), Toronto, Canada M5B 1W8;

10. Procter & Gamble Pharmaceuticals Health Care Research Center (A.B., C.R., J.L.), Mason, Ohio 45040;

11. The Jean Hailes Foundation, Research Unit (S.D.), Clayton, Australia VIC 3168;

12. Department of Medicine (S.D.), Monash University, Praham, Victoria, Australia VIC 3800

Abstract

Abstract 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 μg/d (n = 283) was administered. There were 19 patients who withdrew due to adverse events in the placebo group and 24 in the 300 μg/d testosterone group. Intervention: Testosterone (300 μg/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.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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