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临床试验/IRCT2016051215281N9
IRCT2016051215281N9已完成未知

Comparison of effect of intravenous administration of Lidocaine-Fentanyl and lidocaine on reduction of propofol induced pain during intravenous injection

Vice chancellor for International branch of Shiraz Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
150

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
15 years 至 74 years(—)
性别
All

入选标准

  • patients should be 16-74 years of age, they shouldn't have any cardiovascular, autoimmune disease and diabetes.

排除标准

  • patients who received sedative drugs 24 hours prior to surgery, any drug allergy, neurologic and/or psychologic disease, drug addicts, pregnant women,patients requiring rapid induction of anesthesia.

研究者

发起方
Vice chancellor for International branch of Shiraz Medical Sciences

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