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临床试验/NCT01595711
NCT01595711终止不适用

Prediction of the Occurrence of Chronic Pain After Thoracotomy by Measuring Preoperative Skin Conductance (Pain Monitor Device)

Hopital Foch2 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2012年3月7日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Hopital Foch
入组人数
6
试验地点
2
主要终点
Prediction of chronic pain

研究概览

简要总结

The skin conductance algesimeter (Pain Monitor™, Med-Storm Innovation AS, NO-0264 Oslo, Norway)) reflects the sympathetic nervous system by the measurement of the skin conductance of the palm of the hand. SCA detects nociceptive pain fast and continuously, specific to the individual, with higher sensitivity and specificity than other available objective methods.

The skin conductance response to a calibrated noxious stimulus varies among patients. It defines two types of people depending on its magnitude.

The investigators assume that the importance of skin conductance response to a noxious stimulus predicts the occurrence of chronic pain in patients operated by thoracotomy.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult patients of both sexes
  • planned pulmonary resection for cancer performed by a posterolateral thoracotomy
  • thoracic epidural analgesia

排除标准

  • pregnancy,
  • morbid obesity,
  • insulin-dependent diabetes with dysautonomia,
  • inability to proceed with anesthesia using the BIS signal,
  • known allergy to remifentanil, propofol, atracurium or to levobupivacaine,
  • contra-indication to nefopam
  • contra-indication to ketoprofen

结局指标

主要结局

Prediction of chronic pain

时间窗: one year after surgery

Prediction of chronic pain by the measurement of skin conductance

次要结局

  • Prediction of the postoperative pain(5 days postoperatively)
  • Prediction of the postoperative antalgic requirement by the genetic study(One year after surgery)
  • Prediction of the postoperative antalgic requirement(5 days postoperatively)
  • Effect of remifentanil on skin conductance(One hour after anesthesia)

研究者

发起方
Hopital Foch
申办方类型
Other
责任方
Sponsor

研究点 (2)

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