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临床试验/IRCT20141209020258N83
IRCT20141209020258N83招募中2 期

comparison of adding dexmedetomidine and tramadol and neostigmine to ?lidocaine 1.5% for reduce postoprative pain in caudal block in 2-8 children ?lower abdominal surgeries?

Arak University of Medical Sciences0 个研究点目标入组 96 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
入组人数
96

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
2 years 至 8 years(—)
性别
All

入选标准

  • Children 8-2 years old
  • ASA class I and II
  • All patients without heart disease, pulmonary, liver and ...
  • Patients without seizure history
  • Patients who duration of operation is between 45- 90 minutes
  • Local anesthetics, dimethomidine, tramadol and neostigmine

排除标准

  • All patients with a duration of more than 90 minutes.
  • All patients with failure in codal block

研究者

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