NCT02663284已完成不适用
Evaluation of Non-invasive Monitor of Physiodoloris Pain in Patients With Complex Regional Pain Syndrome Treated by Nerve Block (Prospective Monocenter Study)
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Hopital Foch
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Evaluation of ANI before the peri-neural block
研究概览
简要总结
A French University team (M. Jeanne, MD, and M. LOGIER, Ph D) have developed a pain assessment tool based on the analysis of the variability heart rate which evaluates the Analgesia Nociception Index (ANI). This index is intended to give a quantification of pain.
The aim of the present study is to assess the validity of the ANI parameter in patients with Complex Regional Pain Syndrome treated with a nerve block (reversible pain).
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 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
- 否
入选标准
- •patients suffering from a Complex Regional Pain Syndrome of the upper or lower limb
排除标准
- •contra-indication of a nerve block,
- •contra-indication of the use of the pain monitor
研究组 & 干预措施
Perineural block
Experimental
Perineural block with Ropivacaine 0.5%
干预措施: Ropivacaine 0.5% (Drug)
结局指标
主要结局
Evaluation of ANI before the peri-neural block
时间窗: 5 minutes
ANI is recorded before each nerve block
Evaluation of pain before the peri-neural block
时间窗: 5 minutes
Pain score is recorded before each nerve block
次要结局
- Evaluation of ANI after the peri-neural block(10 minutes)
- Evaluation of pain after the peri-neural block(10 minutes)
研究者
研究点 (1)
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