跳至主要内容
临床试验/NCT00282997
NCT00282997已完成3 期

A 12-Week, Open-Label, Safety Trial Of Pregabalin In Patients With Fibromyalgia

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.72 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2006年2月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
500
试验地点
72
主要终点
To evaluate the safety of pregabalin in patients with fibromyalgia

研究概览

简要总结

To evaluate the safety of pregabalin in patients with fibromyalgia.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients must meet the ACR criteria for fibromyalgia (ie, widespread pain present for at least 3 months, and pain in at least 11 of 18 specific tender point sites.
  • Patients must complete the double-blind study.

排除标准

  • Patients who experienced a serious adverse event during the previous fibromyalgia study, which was determined to be related to the study medication.

结局指标

主要结局

To evaluate the safety of pregabalin in patients with fibromyalgia

次要结局

未报告次要终点

研究者

发起方
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (72)

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