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临床试验/IRCT20190109042309N2
IRCT20190109042309N2已完成3 期

Comparison of the effect of Hyoscine N-Butylbromide and Lidocaine 2% on the propofol injection pain

Sabzevar University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
80

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

  • The patient is a candidate for general anesthetic and surgery
  • ages 18and 65
  • Ability to communicate with the research team
  • Having at least a fifth grade of elementary school
  • American Society of Anesthesiology Class I, II
  • patient has the consent and willingness to participate in the research

排除标准

  • Sensitive to the drugs studied
  • Having Nervous-Muscular Diseases
  • Having heart disease and history of seizures
  • Having metabolic and gastrointestinal disorders
  • Severe nervous and psychiatric disorders
  • Need for induction of anesthesia and rapid intubation
  • Kidney disease in the final stage
  • Liver disorders

研究者

发起方
Sabzevar University of Medical Sciences

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