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临床试验/NL-OMON38660
NL-OMON38660已完成不适用

Comparison of Adequacy of Anesthesia Monitoring with Standard Clinical Practice during Routine General Anesthesia - 123.04-2012-GES-0009

GE Healthcare Attn: Petra Peltola, Clinical Research Manager0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • Age 18-80 years of age
  • Surgery that is expected to last at least 2 hours under general anesthesia with endotracheal tube

排除标准

  • Any subject with a cardiac pacemaker
  • Any subject with atrial fibrillation at the time of obtaining the baseline values
  • Any subject with more than 5 ventricular extra systoles/minute at the time of obtaining the baseline values
  • Any subject who needs invasive blood pressure measurement
  • Any subject who show hemodynamics that would have qualified for being considered as a sign of inadequate anesthesia already at baseline
  • Any subject with epidural anesthesia or analgesia during the surgery. Epidural catheter may be placed pre-operatively, and used in the PACU, but not during the surgery
  • Any subject having surgery that requires prone position
  • Any subject with very high body mass index (>35) because of incompatibility with the target controlled anesthesia models used
  • Any subject with known allergies to the specific anesthetic agents/ analgesic drugs intended for use in their surgeries
  • Any subject with laryngeal mask airway
  • Any subject who is going to have major surgery with a high risk of extensive blood loss
  • Any subject with known chronic use of opioids

研究者

发起方
GE Healthcare Attn: Petra Peltola, Clinical Research Manager

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