跳至主要内容
临床试验/NCT00264628
NCT00264628已完成不适用

An Outpatient, Randomised, Double-blind, Placebo Controlled, Parallel Group Exploratory Study to Evaluate Safety, Tolerability and Efficacy of GW679769 in Patients With Fibromyalgia Syndrome Comorbid With Depression.

GlaxoSmithKline0 个研究点目标入组 8 人开始时间: 2005年10月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
8
主要终点
Change in Fibromyalgia Impact Questionnaire (FIQ) total score

研究概览

简要总结

The purpose of the study is to investigate safety, tolerability and efficacy of oral GW679769 up to 120 mg dose compared to placebo in patients with ACR(American College of Rheumatology)-defined fibromyalgia, co-morbid with depression.

研究设计

研究类型
Observational

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Change in Fibromyalgia Impact Questionnaire (FIQ) total score

时间窗: throughout study

次要结局

  • Effect of GW679769 vs placebo in health-related quality of life outcomes(throughout study)
  • Relationship between PK of GW679769 and clinical outcome in patients(throughout study)
  • Safety and Tolerability(throughout study)

研究者

申办方类型
Industry
责任方
Sponsor

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