Ultra-protective Ventilation Monitored by Electrical Impedance Tomography in Patients With Severe Acute Respiratory Distress Syndrome on Veno-venous ECMO (EIT-ECMO)
Severe ARDS
About this trial
This is an interventional other trial for Severe ARDS focused on measuring ECMO, ARDS, ultra-protective mechanical ventilation
Eligibility Criteria
Inclusion Criteria: aged ≥ 18 years patient with ARDS on venovenous (VV)-ECMO Written informed consent patient affiliated to a social security scheme Exclusion Criteria: Pregnancy Adult patient subject to a legal protection measure (tutor, curator, etc.) Patients with a pacemaker, automatic implantable cardioverter defibrillator, contraindications to thoracic belt placement (e.g., thoracic or spinal cord trauma, recent thoracic surgery) undrained pneumothorax, bronchopleural fistula hemodynamic instability (i.e., use of intravenous fluids of more than 10 mL/kg or vasopressors 2 mg/h of norepinephrine or 0.5 mg/h of epinephrine)
Sites / Locations
- Service de médecine intensive - réanimation Hopital Pitié SalpêtrièreRecruiting
Arms of the Study
Arm 1
Experimental
Interventional
All patients included