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临床试验/IRCT2016112224606N2
IRCT2016112224606N2已完成2 期

Comparison of propofol and fentanyl with propofol and ketamine in sedation and analgesia in trauma patients

Vice chancellor for researche, Mazandaran University of Medical Siences0 个研究点目标入组 132 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
132

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 60 years(—)
性别
All

入选标准

  • inclusion criteria:
  • 1. Age between 18 and 60 years, have indicated a painful procedure and this treatment included painful reduction of dislocation and fractures can be done in an emergency.
  • 2 Persons according to the American Society of Anesthesiologists Physical Status Classification (ASA) class 1 and 2 have
  • Exclusion criteria:
  • 1 - persons under 18 years and above 60 years of age
  • 2- people with Anesthesiologists Physical Status Classification (ASA) class more than two
  • 3-people with kidney and liver disease
  • 4-person with alcohol consumption
  • 5-people addicted to drugs
  • 6- pregnant and lactating women
  • 7- those who have contraindications to the use of ketamine and propofol and fentanyl

排除标准

  • 未提供

研究者

发起方
Vice chancellor for researche, Mazandaran University of Medical Siences

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