NL-OMON24168尚未招募不适用
Percutaneous sympathetic blockade in complex regional pain syndrome type 1;A prospective clinical investigation on predictors of sympatheticaly maintained pain.
Department of Anesthesiology, the Academic Hospital Maastricht0 个研究点目标入组 124 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 124
研究概览
简要总结
/A
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •Adult (18 years or more) male or female patiënts with CRPS1 as diagnosed by IASP criteria, with a duration of 12 months or less with moderate to severe pain (mean NRS of more than 4 in the previous week as measured 3 times daily in a pain diary with 0=no pain and 10= worst imaginable pain) and one extremity involved.
排除标准
- •1. Patiënts 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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