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According to the ARDS Berlin definition, patients with severe concurrent invasive mechanical ventilation were selected, and clinical data and prognosis were collected. Samples such as blood and balf were collected for analysis based on changes in the condition.
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Exclusion criteria
Patients with intracranial hypertension, pleural fistula, pneumothorax, HIV, HBV, HCV
Age>85 years old or<18 years old
Pregnant patients
Severe hemodynamic instability (vasopressor increase>30% in the first 6 hours, or Norepinephrine>0.5 mg kg/min)
Patients unable to perform EIT ventilation and/or perfusion testing (unable to perform internal jugular vein catheterization, Hypernatremia, chest malformation, active implant device, unstable spinal injury or fracture, skin lesions opposite the EIT monitoring area)
Patients with abnormal esophageal anatomical structure and inability to indwelling gastric tubes
Disagreement for inclusion in this study
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Central trial contact
Lin Wang, doctor
Data sourced from clinicaltrials.gov
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