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临床试验/NCT02844894
NCT02844894Unknown4 期

The Effects of Preintubation Esmolol and and Dexmedotimidine on Ischmeia Modified Albumin Levels

Ufuk University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
60
试验地点
1
主要终点
ischemia modified albumine

研究概览

简要总结

This study investigates the effects of dexmedetomidine and esmolol given intravenously before intubation on sympathetic response caused by intubation itself. Half the patients will recevice dexmedetomidine and the other half will receive dexmedetomidine. Ischemia modified albumine levels will be measured

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients undergoing elective surgery under general anesthesia

排除标准

  • Patient refusal
  • Morbid obesity (BMI>30)
  • Advanced systemic disease
  • Hypoalbumiemia
  • beta-blocker usage
  • Anticipated difficult ventilation and/or intubation

研究组 & 干预措施

dexmedetomidine

Experimental

0.5 mcg/kg dexmedetomidine in 20 ml normal saline will be infused in 5 minutes before intubation

干预措施: Dexmedetomidine (Drug)

Esmolol

Experimental

0.5 mg/kg esmolol in 20 ml normal saline will be infused in 5 minutes before intubation

干预措施: Esmolol (Drug)

Placebo

Placebo Comparator

20 ml normal saline infused in 5 minutes before intubation

干预措施: Placebo (Drug)

结局指标

主要结局

ischemia modified albumine

时间窗: 10 minutes after endotracheal intubation

ischemia modified albumine levels will be measured as a response to intubation

次要结局

未报告次要终点

研究者

发起方
Ufuk University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Perihan Ekmekçi

Associate Professor

Ufuk University

研究点 (1)

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