跳至主要内容
临床试验/NCT00657501
NCT00657501已完成3 期

A Phase III, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study of the Safety and Efficacy of LibiGel® for the Treatment of Hypoactive Sexual Desire Disorder in Surgically Menopausal Women

BioSante Pharmaceuticals69 个研究点 分布在 1 个国家目标入组 575 人开始时间: 2008年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
575
试验地点
69
主要终点
Co-primary endpoints are the change in the 4-week total number of satisfying sexual events from the Baseline period to Weeks 21-24, and the change from Baseline to Weeks 21-24 in the mean ISED desire score.

研究概览

简要总结

This study is a randomized, double-blind, placebo-controlled, multi-center study of the safety and efficacy of LibiGel 300mcg in the treatment of HSDD in surgically menopausal women.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
30 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Must be between the ages of 30 to 65 years
  • Must have undergone hysterectomy and bilateral salpingo-oophorectomy

排除标准

  • A history of allergic reactions to androgens (oral or patch), topical alcohol, or any component of the formulation
  • Any systemic skin diseases or local skin abnormalities in the area of application
  • Diagnosed with another primary female sexual dysfunction (e.g., Sexual Aversion Disorder, Female Sexual Arousal Disorder).
  • A medical condition that could affect or interfere with sexual function
  • Using a systemic transdermal gel or cream estrogen therapy.

研究组 & 干预措施

testosterone gel

Experimental

1% testosterone transdermal gel

干预措施: testosterone gel (Drug)

Placebo gel

Placebo Comparator

placebo transdermal gel

干预措施: placebo gel (Drug)

结局指标

主要结局

Co-primary endpoints are the change in the 4-week total number of satisfying sexual events from the Baseline period to Weeks 21-24, and the change from Baseline to Weeks 21-24 in the mean ISED desire score.

时间窗: Time Frame: Baseline and 21-24 weeks.

次要结局

  • Change from baseline over time for multiple efficacy measurements(change over timepoints from baseline period)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (69)

Loading locations...

相似试验