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临床试验/IRCT20240207060924N1
IRCT20240207060924N1招募中3 期

Comparison of outcomes between Propofol and Dexmedetomidine on extubation time and vital signs in patients with post- coronary artery bypass grafting in Open heart Intensive Care Unit

Arak University of Medical Sciences0 个研究点目标入组 92 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
92

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
35 years 至 80 years(—)
性别
All

入选标准

  • Having informed consent
  • Patients must meet inclusion criteria, i.e. be elective and referred for open heart surgery only
  • Age should be between 35 and 80 years old
  • Performed by the same surgeon
  • The maximum duration of the surgery must be 6 hours
  • All were operated with a cardiopulmonary pump
  • Valve surgery should not be performed at the same time as CABG

排除标准

  • Patient is not a candidate for elective CABG surgery
  • Duration of surgery is more than 6 hours
  • Patients have not had surgery outside of the cardiopulmonary pump
  • Patients outside the 35-80 age range
  • The patient has the right to withdraw at any stage of the research

研究者

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