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临床试验/IRCT20200803048288N1
IRCT20200803048288N1已完成3 期

Comparative study of the effect of Haloperidol and Dexmedetomidine on delirium and agitation in mechanically ventilated patients following concussion admitted to the intensive care unit

Ahvaz University of Medical Sciences0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
入组人数
60

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
18 years 至 65 years(—)
性别
All

入选标准

  • APACHE II criteria more than 48
  • RASS criteria between +1 to +4
  • At least 48 hours after hospitalization in the intensive care unit

排除标准

  • Dissatisfaction of the patient's legal guardian
  • Patients who are candidates for surgery
  • Unstable hemodynamic status
  • History of mental illness or use of neuroleptics
  • History of drug use any contraindications to Dexmedetomidine or Haloperidol (Allergy, Parkinson's, Hypotension, BradyCardiac)
  • Renal or Hepatic Fysfunction

研究者

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