跳至主要内容
临床试验/CTRI/2023/10/058352
CTRI/2023/10/058352尚未招募4 期

A non-inferiority, randomized, controlled trial comparing high flow nasal cannula to non-invasive ventilation in patients with acute cardiogenic pulmonary edema in emergency room - nil

AIIMS BHUBANESWAR0 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
4 期
状态
尚未招募

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

  • 1.Patients of age 18 to 80years, presenting to Emergency department with acute dyspnea, with clinical, radiological and ultrasonography evidence of acute cardiogenic pulmonary edema.
  • 2.The patient must have substantial breathing difficulties that necessitate the use of non-invasive ventilation techniques to provide relief which is assessed by following criteria
  • 2.1 Respiratory rate(RR) >25 breaths/min with signs of respiratory distress such as, use of accessory muscles of respiration
  • 2.2 SpO2 <90% on room air,PaO2/FiO2 <200 with maximum oxygen supplementation by conventional methods.

排除标准

  • 1.Patients needing immediate endotracheal intubation due to severe respiratory distress and inability to maintain adequate oxygenation(SpO2 <90% with oxygen supplementation)
  • 2.Patients with cardiac or respiratory arrest
  • 3.Patients with hemodynamic instability
  • 4.Patients with a low Glasgow Coma Scale score <10
  • 5.Patients having excessive respiratory secretions
  • 6.Agitated/Non-cooperative patients
  • 7.Patients associated with pulmonary diseases like AECOPD/pneumonia/interstitial lung disease/pneumothorax/lung metastasis/miliary TB
  • 8.Patients with fluid overload due to chronic kidney disease
  • 9.Patients with acute myocardial infarction
  • 10.Patients with do-not-intubate order
  • 11.Patients with home NIV support
  • 12.Pregnant patients

研究者

相似试验