ISRCTN71968956已完成未知
Percutaneous sympathetic blockade in complex regional pain syndrome type 1: a prospective clinical investigation on predictors of sympatheticaly maintained pain
Academic Hospital Maastricht (AZM) and Dutch Consortium for Research on Trauma Related Neuronal Dysfunction (TREND)0 个研究点目标入组 49 人开始时间: 2006年6月7日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 49
研究概览
简要总结
2012 results in: https://www.ncbi.nlm.nih.gov/pubmed/22143169 (added 02/05/2019)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Adult (18 years or more) male or female patients with CRPS1 as diagnosed by International Association for the Study of Pain (IASP) criteria, with a duration of 12 months or less with moderate to severe pain (mean numerical rating scale [NRS] of more than 4 in the previous week as measured three times daily in a pain diary where, 0 = no pain and 10 = worst imaginable pain) and one extremity involved.
排除标准
- •1. Patients of less than 18 years of age
- •2. The existence of significant impairment of blood coagulation or the use of oral anticoagulant medication
- •3. Patients suffering from diabetic polyneuropathia
- •4. Patients who are unlikely to comply with study requirements
- •5. Pregnant women
- •6. CRPS1 with a duration of more than 12 months
研究者
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