ISRCTN43633981已完成不适用
Intrathecal Baclofen Infusion for Reflex sympathetic Dystrophy related dystonia
eiden University Medical Centre (LUMC) (The Netherlands)0 个研究点目标入组 45 人开始时间: 2007年2月26日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 45
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •1. All patients should fulfill the diagnostic criteria of the complex regional pain syndrome consensus report of the International Association for the Study of Pain (IASP):
- •1.1. Continuing pain, allodynia or hyperalgesia, in which the pain is disproportionate to any inciting event
- •1.2. Evidence at some time of oedema, changes in skin blood flow, or abnormal sudomotor activity in the region of the pain
- •1.3. No condition that would otherwise account for the degree of pain and dysfunction
- •2. All patients must suffer from tonic dystonia in one or more extremities, that may cause fixed postures at rest of variable severity
- •3. Before starting the study all patients will have received a trial with oral baclofen. Only patients with an insufficient response or dose-limiting sedative effects to oral baclofen are eligible for this study
排除标准
- •Does not comply with the above inclusion criteria
研究者
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