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临床试验/NL-OMON53828
NL-OMON53828招募中不适用

Flow versus Pressure Controlled Ventilation in patients with moderate to severe Acute Respiratory Distress Syndrome - FCV vs PCV in moderate to severe ARDS

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 28 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
28

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

年龄范围
18 至 99(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • - 18 years or older;
  • - Provided written informed consent;
  • - Undergoing controlled mechanical ventilation via an endotracheal tube;
  • - Meeting all criteria of the Berlin definition of ARDS:
  • o Hypoxic respiratory failure within 1 week of a known clinical insult or new
  • or worsening respiratory symptoms
  • o Bilateral opacities on X-ray or CT-scan not fully explained by effusions,
  • lobar/lung collapse (atelectasis), or nodules
  • o Respiratory failure not fully explained by cardiac failure or fluid overload.
  • o Oxygenation: moderate ARDS P/F ratio between 101-200 mmHg, severe ARDS PF
  • ratio <= 100mmHg, both with PEEP >= 5 cmH2O.
  • - Development of ARDS <= 72 uur
  • - Intubated

排除标准

  • - Severe sputum stasis or production requiring frequent bronchial suctioning
  • (more than 5 times per nurse shift) - Untreated pneumothorax (i.e. no pleural
  • drainage) - Hemodynamic instability defined as a mean arterial pressure below
  • 60mmHg not responding to fluids and/or vasopressors or a noradrenalin dose >
  • 0.5mcrg/kg/min - High (>15 mmHg) or instable (an increase in sedation or
  • osmotherapy is required) intracranial pressure - An inner tube diameter of 6mm
  • or less - Anticipating withdrawal of life support and/or shift to palliation as
  • the goal of care - Inability to perform adequate electrical impedance
  • tomography (EIT) measurements - Contra-indications for nasogastric tube or
  • inability to perform adequate transpulmonary pressure measurements

研究者

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