Effect of PEEP Titration on the EELV Measured by the Nitrogen Dilution Technique in ARDS

Last updated: April 16, 2020
Sponsor: Centre Hospitalier Intercommunal Aix-Pertuis
Overall Status: Active - Recruiting

Phase

N/A

Condition

Lung Injury

Acute Respiratory Distress Syndrome (Ards)

Treatment

N/A

Clinical Study ID

NCT04352725
20192211-1
  • Ages > 18
  • All Genders

Study Summary

Mechanical ventilation of the patient with acute respiratory distress syndrome is one of the first therapies.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients admitted to intensive care with a diagnosis of moderate to severe ARDS inaccordance with the Berlin criteria, i.e. a PAFI <200 and PEEP >5cm H20 ratio

  • Diagnosis of ARDS made within 72 hours

  • Age over 18 years

  • Informed consent of the patient and/or trusted person where applicable

Exclusion

Exclusion Criteria:

  • Start of mechanical ventilation more than 72 hours prior to inclusion.

  • SDRA evolving for more than 72 hours

  • Presence of major hemodynamic instability with mean blood pressure <60mmhg, and/orheart rate <45 bpm or >150bpm with an increase in vasopressor amine dosage of morethan 20% over the last 6 hours.

  • Intracranial hypertension with CPP<60mmhg

  • Massive hemoptysis requiring immediate surgical or interventional radiology procedure

  • Tracheal surgery (except intensive care tracheotomy) or sternotomy within the previous 15 days

  • Trauma or surgery of the face in the previous 15 days.

  • Deep vein thrombosis treated for less than 2 days

  • Pacemaker implantation in the last 2 days

  • Unstable fracture (spine, femur or pelvis)

  • Respiratory reasons

  • use of extracorporeal oxygenation

  • nitric oxide

  • pleural drainage system with bronchopleural gap

  • pulmonary transplantation

  • Poor respiratory tolerance per procedure with desaturation Spo2<85%.

  • Poor hemodynamic tolerability per procedure combining hypotension with MAP<65mmhg anda 20% increase in norepinephrine dosage.

  • Lack of patient consent to proceed

  • minor patient

  • lack of consent

Study Design

Total Participants: 40
Study Start date:
January 20, 2020
Estimated Completion Date:
November 30, 2020

Study Description

The application of positive end expiratory pressure is recommended but the question remains "How to set the best positive end-expiratory pressure (PEEP) level for each patient? ". Different titration techniques have been studied on oxygenation and respiratory mechanics parameters without reaching a consensus. Currently we have a module that is connected to the ventilator to collect the patient's lung volume. It will therefore allow us to optimize the settings of the ventilator and to set the best level of positive end-expiratory pressure "best peep" in order to individualize our treatment for each patient.

Connect with a study center

  • Centre Hospitalier Intercommunal Aix-Pertuis

    Aix-en-Provence, 13100
    France

    Active - Recruiting

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