跳至主要内容
临床试验/CTRI/2013/03/003462
CTRI/2013/03/003462已完成4 期

A dose response study of caudal dexmedetomidine with ropivacaine in pediatric patients undergoing lower abdominal and perineal surgery

Director0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
80

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

入选标准

  • eighty ASA physical status I-II children, aged 1 to 8 years, undergoing lower abdominal and perineal surgery

排除标准

  • Contraindication to caudal block (infection at site of block, bleeding diathesis, preexisting Neurological/ Spinal disease or abnormality of sacrum)
  • Children with conduction blocks.
  • History of allergic reaction to local anaesthetics or the study drugs.
  • History of developmental delay/mental retardation

研究者

发起方
Director

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