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临床试验/CTRI/2012/09/002948
CTRI/2012/09/002948已完成4 期

Safety and Effectiveness of Dexmedetomidine for sedation during awake nasal fibreoptic intubation ? A prospective, randomized, double blind study

Kasturba Hospital KMC Manipal0 个研究点目标入组 36 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
36

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

  • All patients between 18-85 years undergoing awake nasal fibreoptic intubation

排除标准

  • ASA physical status IV
  • Raised intracranial pressure
  • Uncontrolled seizure disorder and/or known psychiatric illness
  • Current (in the past 14 days) treatment with an α2 agonist or antagonist
  • Patients in whom dexmedetomidine or benzodiazepine administration is contra-indicated
  • Patients with acute unstable angina, laboratory confirmed acute myocardial infarction within the past 6 weeks, heart rate < 50 bpm, systolic blood pressure (SBP) < 90 mmHg, or complete heart block unless they have a pacemaker
  • Patients with elevated SGPT (ALT) and/or SGOT (AST) values of > 2 times the upper limit of normal.

研究者

发起方
Kasturba Hospital KMC Manipal

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