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临床试验/NL-OMON33353
NL-OMON33353已完成不适用

Measurement of nociception and prediction of movement during combined general (sevoflurane/fentanyl)-epidural anesthesia in ASA I-III patients undergoing major abdominal surgery using bilateral frontal EEG measurements and hemodynamic parameters (pulse transit time, cardiac output, blood pressure and heart rate) - CVI

eids Universitair Medisch Centrum0 个研究点目标入组 90 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
90

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 至 99(—)

入选标准

  • Age: 18-80 years;
  • Sex: male or female;
  • Surgery: elective abdominal surgery lasting at least 2 hours. This includes gynecological procedures (eg., abdominal hysterectomies), urological procedures (eg., radical prostatectomies), GI-surgery (eg., colon surgery);
  • ASA status: 1, 2 or 3.

排除标准

  • Age: < 18 or > 80 years;
  • Unable to give written informed consent;
  • Pregnancy/lactation;
  • Extreme obesity: BMI > 35;
  • Perceived difficult intubation requiring muscle relaxation.

研究者

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Measurement of nociception and prediction of... | 临床试验