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临床试验/CTRI/2022/04/042249
CTRI/2022/04/042249已完成未知

Comparison of the efficacy of Intranasal Atomised Dexmedetomidine versus Intranasal Atomised ketamine as a premedicant for anxiolysis and sedation in paediatric population aged 1-10 years undergoing spinal dysraphism surgery - a randomised double blinded controlled trial.

Ankur Luthra0 个研究点目标入组 64 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
Ankur Luthra
入组人数
64

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

  • 64 ASA I and II children aged between 1-10years scheduled for spinal dysraphism surgery will be enrolled in this study.

排除标准

  • Refusal of consent
  • Known allergy to dexmedetomidine or ketamine
  • ASA III or IV
  • Children with cardiac anomalies
  • Children with seizures
  • Children with upper respiratory tract infection
  • Children with liver disease
  • Children with mental retardation
  • Difficult cannulation (three or more attempts)

研究者

发起方
Ankur Luthra

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