Endometrial Safety Study of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women

Completed · Phase 3 · Has a placebo group

Conditions studied: Hypoactive Sexual Desire Disorder

In brief

This study is designed to evaluate the endometrial safety of a testosterone patch as treatment for low libido in naturally postmenopausal women.

Key facts

Study ID

NCT00467259

Run by

Warner Chilcott

People needed

1271

Starts

2007-04-01

Expected to finish

2009-01-01

Last updated by the study team

2011-12-15

Who can join

Age: 45 and older, up to 70. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women will be screened for study participation and must be at least one year post menopausal, 45-70 years old, in general good health, and may or may not be on hormone therapy, and must have low sexual desire which causes distress.

You may not qualify if…

• Women will be screened for study participation and must not be using androgen therapy or have any medical, physical, psychological, or pharmacological condition that could make participation unsafe or confound the safety evaluation.

Where it is running

• Research Facility — Birmingham, Alabama, United States
• Research Facility — Mobile, Alabama, United States
• Research Facility — Montgomery, Alabama, United States
• Test Facility — Chandler, Arizona, United States
• Study Facility — Peoria, Arizona, United States
• Research Facility — Phoenix, Arizona, United States
• Research Facility — Phoenix, Arizona, United States
• Research Facility — Scottsdale, Arizona, United States
• Research Site — Tucson, Arizona, United States
• Research Facility — Tucson, Arizona, United States
• Study Facility — Tuscon, Arizona, United States
• Site Facility — Jonesboro, Arkansas, United States
• Site Facility — Little Rock, Arkansas, United States
• Research Facility — Anaheim, California, United States
• Research Site — Berkeley, California, United States
• Research Facility — Palm Desert, California, United States
• Research Facility — Pasadena, California, United States
• Research Facility — San Diego, California, United States
• Research Facility — San Ramon, California, United States
• Test Facility — Santa Rosa, California, United States
• Site Facility — Upland, California, United States
• Research Facility — Vista, California, United States
• Site Facility — Vista, California, United States
• Site Facility — Westlake Village, California, United States
• Study Facility — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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