IRCT201209053104N2已完成2 期
Comparing the effectiveness of adding paracetamol and dexamethasone to lidocaine for intravenous block of upper extremity on severity of pain and period ?of painless during and after surgery.?? ?
Vice chancellor for research, Kerman University of Medical Sciences0 个研究点目标入组 60 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
- 60
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
- 20 years 至 60 years（—）
- 性别
- All
入选标准
- •20 to 60 years old; candidate for upper extremity surgery and ASA I or II.
- •Exclusion criteria:
- •Lidocaine allergy; infection; open fracture of limb; liver disease and addiction to opium and alcohol
排除标准
- 未提供
研究者
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