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Safety and Efficacy of LibiGel® for Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women — BLOOM  

Hypoactive Sexual Desire Disorder Clinical Trial

Official title:
A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study of the Long-Term Safety and Efficacy of LibiGel® for the Treatment of Hypoactive Sexual Desire Disorder in Postmenopausal Women

Clinical Trial Summary

This study is a randomized, double-blind, placebo-controlled, adaptive design, multi-center study of the long-term cardiovascular and breast safety of LibiGel in the treatment of HSDD in postmenopausal women with at least two points of cardiovascular risk and clinical diagnosis of Hypoactive Sexual Desire Disorder (HSDD).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Disease
  • Hypoactive Sexual Desire Disorder
  • Hypokinesia
  • Sexual Dysfunctions, Psychological
Clinical Trial Details
NCT number NCT00612742
Study type Interventional
Source BioSante Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date January 2008
Completion date December 2012
View Details
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