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临床试验/CTRI/2021/06/034309
CTRI/2021/06/034309已完成未知

A comparative study of the efficacy and safety profile of intravenous versus nebulized Dexmedetomidine in attenuation of haemodynamic response to direct laryngoscopy and endotracheal intubation.

Arindam Chatterjee0 个研究点目标入组 50 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
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • American Society of Anaesthesiologists(ASA) physical status I and II.
  • Aged between 18 and 60 years.
  • Undergoing elective surgery under general anaesthesia with endotracheal intubation.

排除标准

  • Known allergy to Dexmedetomidine.
  • ASA III and IV.
  • Predicted difficult airway planned for awake intubation.
  • Emergency surgeries.
  • Pregnant patients.
  • Patients on treatment with beta blockers or other rate control drugs, pacemakers.
  • Patient refusal to participate in the study.

研究者

发起方
Arindam Chatterjee

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