跳至主要内容
临床试验/NCT00541476
NCT00541476已完成不适用

Non-Interventional Study In Patients With Peripheral Or Central Neuropathic Pain Undergoing Symptomatic Treatment With Lyrica

Pfizer's Upjohn has merged with Mylan to form Viatris Inc.0 个研究点目标入组 746 人开始时间: 2007年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
746

研究概览

简要总结

The purpose of this study is to obtain more data about efficacy and safety of the study drug Lyrica.

研究设计

研究类型
Observational
时间视角
Prospective

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

  • Clinical diagnosis of peripheral or central neuropathic pain

排除标准

  • None. Patients recruited by physician decision. Patient's personal data are not collected.

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

相似试验