跳至主要内容
临床试验/CTRI/2018/02/012076
CTRI/2018/02/012076尚未招募未知

A Prospective Randomized study to compare the efficacy of Propofol-Ketamine combination with Dexmedetomidine for performing Drug Induced Sleep Endoscopy(DISE) in patients of Obstructive Sleep Apnoea.

TATA Motors Hospital0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
发起方

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 who give their informed consent willingly.
  • Clinical symptoms of snoring, morning headaches,tiredness,daytime sleepiness.
  • ASA status 1-2.
  • Apnoea-Hypopnea Index (AHI) score greater than 5 events per hour on Polysomnography.
  • No active focus of infection in nose and throat.
  • All patients who have previously failed to respond to conservative treatment for OSA, like changes in sleep position and sleep hygiene.
  • Patients who were either intolerant or unwillingly to use continuous positive airway pressure therapy.
  • Patients with no major systemic disease.

排除标准

  • Age < 18 years and >60 years.
  • Patients with high ASA score >3.
  • Severe OSA (AHI >70 events/hour).
  • Morbid Obesity BMI >30kg/m2.
  • Patients with 2nd-3rd degree A-V block.
  • Known allergies against the study drugs.
  • Gross maxillary and mandibular deformities (mainly retrognathia) on lateral cephalometry.
  • Patients with psychiatric disorders.
  • Patients who have undergone previous surgical therapies for OSA.
  • Mallampati score of 3-4.
  • History of drug or alcohol abuse.
  • History of chronic alcohol use.

研究者

发起方
TATA Motors Hospital

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