IRCT2017060620258N49招募中2 期
Compared the effects of adding Dexmedetomidine ?and tramadol to lidocaine 5% in the duration of postoperative analgesia in spinal anesthesia in women undergoing cesarean section
Vice Chancellor for Research, Arak University of Medical Sciences0 个研究点目标入组 180 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 180
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 40 years（—）
- 性别
- Female
入选标准
- •20-40 years; cesarean elective candidate Taleghani hosbital; ASA I and II; lack of allergy in Lidocaine and Tramadol and Dexmedetomidine
- •Exclusion criteria: failure in Spinal anesthesia; more than two attempts for spinal anesthesia; prolongation of surgery more than 90 minutes; Patients with substance abuse; patients with cardiovascular and pulmonary
排除标准
- 未提供
研究者
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