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临床试验/NCT02001285
NCT02001285Unknown不适用

Comparison of the Effect-site Concentration of Remifentanil for Blunting Hemodynamic Responses to Ordinary Tracheal and Double-lumen Endobronchial Intubation During Propofol-remifentanil Total Intravenous Anesthesia

Jeju National University School of Medicine1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2013年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
50
试验地点
1
主要终点
arterial blood pressure

研究概览

简要总结

The purpose of this study is the comparison of the effect-site concentration of remifentanil for blunting hemodynamic responses to ordinary tracheal and double-lumen endobronchial intubation during propofol-remifentanil total intravenous anesthesia.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patient who is needed intubation for general anesthesia

排除标准

  • patient who is anticipating difficult airway
  • patient who takes any drug to influence this study
  • cardiovascular disease, renal disease, liver disease

研究组 & 干预措施

Double lumen tube

Experimental

This arm contains patients who are needed endobronchial intubation with double lumen tube for general anesthesia. After propofol infusion of effect site concentration 4 μg/ml, remifentanil infusion will be started with effect site concentration of 3.5 ng/ml. According to change arterial blood pressure and heart rate from baseline value, next remifentanil concentration will be regulated using up-and-down method. Step size of dose is 0.5 ng/ml.

干预措施: Remifentanil (Drug)

single lumen tube

Active Comparator

This arm contains patients who are needed endotracheal intubation with single lumen tube for general anesthesia. After propofol infusion of effect site concentration 4 μg/ml, remifentanil infusion will be started with effect site concentration of 3.5 ng/ml. According to change arterial blood pressure and heart rate from baseline value, next remifentanil concentration will be regulated using up-and-down method. Step size of dose is 0.5 ng/ml.

干预措施: Remifentanil (Drug)

结局指标

主要结局

arterial blood pressure

时间窗: Change from baseline in arterial blood pressure at intubation period

Arterial blood pressure will be recorded before anesthesia, after propofol infusion, after remifentanil infusion and after intubation during 3 min with 1 min interval.

次要结局

  • heart rate(Change from baseline in heart rate at intubation period)

研究者

发起方
Jeju National University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Hyun Jung Kim

Assistant professor

Jeju National University School of Medicine

研究点 (1)

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