IRCT2016040515281N7已完成2 期
Clinical trail comparison of effect of Intravenous administration of Lidocaine with the combination of Sufentanyl and Lidocaine on reduction of Propofol induced pain during intravenous injection on patients candidate for General Surgeries
Vice chancellor for research of International Branch,Shiraz University of 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
- 2 期
- 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
- 16 years 至 65 years（—）
- 性别
- All
入选标准
- •Patients of 16 to 65 y/o admitted for General Surgery. Exclusion criteria: The patients who received sedative drugs 24 hours before operation; Have drug allergy; Patients with Neurological Disorders or Mental disorders; Drug Addicts; Pregnant women; Who requires a rapid induction of anesthesia.
排除标准
- 未提供
研究者
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