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临床试验/DRKS00025762
DRKS00025762已完成不适用

The effect of personalized perioperative blood pressure management on intraoperative cerebral oxygen saturation, burst suppression ratio and postoperative neurological outcomes in patients having major surgery: an observational substudy of the IMPROVE-pilot trial

Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf0 个研究点目标入组 55 人开始时间: 2021年12月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
55

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 one(—)
性别
All

入选标准

  • - American Society of Anesthesiologists physical status class (ASA) II-IV
  • - scheduled for elective major surgery under general anesthesia
  • - surgery expected to last = 120 minutes

排除标准

  • - emergency surgery
  • - patients having liver or kidney transplantation
  • - pregnancy
  • - status of post transplantation of kidney, liver, heart, or lung
  • - sepsis (according to current Sepsis-3 definition)
  • - impossibility of preoperative automated blood pressure monitoring
  • - MAP differences between the right and the left arm of more than 20 mmHg surgery that requires controlled hypotension

研究者

发起方
Zentrum für Anästhesiologie und Intensivmedizin, Universitätsklinikum Hamburg-Eppendorf

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