Personalized Mechanical Ventilation Guided by UltraSound in Patients with Acute Respiratory Distress Syndrome
- Conditions
- Acute respiratory distress syndrome10024967
- Registration Number
- NL-OMON51558
- Lead Sponsor
- Academisch Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 100
Admitted to a participating ICU, invasively ventilated, fulfil the Berlin
criteria for moderate or severe ARDS.
Age under 18, pregnant, participation in an other interventional studie,
conditions in which lung ultrasound is not feasible (e.g. subcutaneous
emphysema, morbid obesity or wounds), mechanical ventilation for longer than 7
consecutive days in the past 30 days, history of ARDS in the previous month,
body-mass index higher than 40 kg/m², intracranial hypertension,
broncho-pleural fistula, chronic respiratory diseases requiring long-term
oxygen therapy or respiratory support, pulmonary fibrosis, patients who are
moribund or facing end of life and no informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method