跳至主要内容
临床试验/ACTRN12618001662257
ACTRN12618001662257招募中未知

The accuracy of the EEG-based qNox monitor to predict moderate-severe acute postoperative pain in peri-operative patients

Prof THomas Ledowski0 个研究点目标入组 150 人开始时间: 2018年10月9日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
150

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

  • Patients at/over 18 years of age scheduled for non-emergency surgery and anaesthesia with sevoflurane/opioid

排除标准

  • Patients will be excluded from further analysis if they lack sufficient English language skills to communicate pain on a self-rated pain scale, have a condition or medication known or suspected of interacting with the acquisition of the eeg data (i.e. know epilepsy, known severe mental disorder), chronic pain (with opioid medication at home), use of ketamine at home or perioperatively within 30 min prior to the commencement of QNOX measurements, abuse of amphetamines or opioids, allergy to sticky tape.

研究者

发起方
Prof THomas Ledowski

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