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临床试验/ACTRN12619001596190
ACTRN12619001596190尚未招募未知

Does intraoperative monitoring of the nociception level index (NOL) allow a prediction of the severity of acute postoperative pain?

Thomas Ledowski0 个研究点目标入组 80 人开始时间: 2019年11月20日最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
80

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 o limit(—)
性别
All

入选标准

  • Adult patients (both sexes) scheduled for non-emergency surgery under general anaesthesia with opioid/sevoflurane at the Royal Perth Hospital

排除标准

  • Patients will be excluded from further analysis if they lack sufficient English language skills to consent and/or to communicate pain on a self-rated pain scale, have a condition or medication known or suspected of interacting with the acquisition of the data (i.e. know severe peripheral neuropathy, known severe mental disorder), chronic pain (with opioid medication at home), use of ketamine at home, abuse of amphetamines or opioids, allergy to sticky tape.

研究者

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