跳至主要内容
临床试验/IRCT20200921048789N2
IRCT20200921048789N2尚未招募3 期

Evaluation of cough frequency and duration of recovery with three anesthesia methods: Propofol + Fentanyl, Propofol + Fentanyl + Lidocaine and Propofol + Fentanyl + Lidocaine + Ketamine in patients referred to the scoping ward

Artesh University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
100

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 70 years(—)
性别
All

入选标准

  • All patients who are candidates for scoping in 501 Army Hospital in 2021

排除标准

  • Age under 18 and over 70 years
  • ASA classification 4 or 5
  • History of uncontrolled blood pressure
  • History of Chronic Obstructive Pulmonary Disease (COPD)
  • History of psychotic or neurological disorders
  • History of seizures
  • History of use of drugs affecting the central nervous system

研究者

发起方
Artesh University of Medical Sciences

相似试验