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
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
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