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临床试验/IRCT20160307026950N21
IRCT20160307026950N21已完成3 期

Study and comparison of two different doses of propofol in prevention of nausea and vomiting in spinal discectomy

Esfahan University of Medical Sciences0 个研究点目标入组 48 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
48

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 person should not have received any sedative or narcotic drugs
  • No gastrointestinal problems such as reflux
  • Patients should be between 18 and 65 years old.
  • Having a informed consent to enter the research

排除标准

  • If there is any change in the relaxation method and the change in the surgical method, the patient should be excluded from the study.
  • The patient's age is more than 65 years
  • The patient's age is less than 18 years

研究者

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