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Continuous Negative Abdominal Pressure in ARDS (CNAP in ARDS)

Acute Respiratory Distress Syndrome

The aim is to test a device for applying continuous negative abdominal pressure in patients with ARDS

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 to 80

Critères de participation

Inclusion Criteria:

1. Patients ≧ 18 years old
2. Patients with moderate to severe ARDS as per the Berlin definition (PaO2/FiO2 ≤200mmHg)
3. Patients with absence of any significant cardiopulmonary disease

Exclusion Criteria:

1. Contraindication to CNAP

a. open abdominal wounds or drainage tubes; b. Acute brain Injury with intracranial pressure \>30 mm Hg or cerebral perfusion pressure \<60 mmHg; c. Decompensated heart insufficiency or acute coronary syndrome; d. Major hemodynamic instability: Mean arterial pressure lower than 60 mm Hg despite adequate fluid resuscitation and two vasopressors or increase of vasopressor dose by 30% in the next 6 hours; f. Unstable spine, femur, or pelvic fractures; g. Pregnancy; h. Pneumothorax;
2. Contraindication to EIT electrode placement: Burns, chest wall bandaging limiting electrode placement
3. Severe liver insufficiency (Child-Pugh score \> 7) or fulminant hepatic failure
4. Major respiratory acidosis or PaCO2 \> 60 mmHg
5. Severe COPD (according to the GOLD criteria defined as severe = FEV1: 30-50% or very severe = FEV1 \< 30%)
6. Clinical judgement of the attending physician

Lieu de l'étude

St. Michael's Hospital
St. Michael's Hospital
Toronto, Ontario
Canada

Contactez l'équipe d'étude

Backup Contact

Laurent Brochard, MD

[email protected]
416 864 5686
Primary Contact

Audery Kim

[email protected]
Étude parrainée par
The Hospital for Sick Children
Participants recherchés
Plus d'informations
ID de l'étude: NCT03425318