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临床试验/IRCT20220221054090N1
IRCT20220221054090N1招募中3 期

Evaluation of the sedative effect of intravenous lidocaine in patients undergoing Endoscopy with Propofol-Ketamine

Ahvaz University of Medical Sciences0 个研究点目标入组 138 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
138

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

  • Candidate patients under 18 to 65 years of age who are in groups 1 and 2 according to the American Society of Anesthesiology (ASA Class)

排除标准

  • Patients with severe heart or lung disease are not included in this study
  • Patients with Renal failure are not included in this study
  • Patients with Liver failure are not included in this study
  • Patients allergic to Propofol, Ketamine, or Lidocaine are not included in this study

研究者

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