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Personalized Mechanical Ventilation Guided by UltraSound in Patients with Acute Respiratory Distress Syndrome

Recruiting
Conditions
Acute respiratory distress syndrome
10024967
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
Inclusion Criteria

Admitted to a participating ICU, invasively ventilated, fulfil the Berlin
criteria for moderate or severe ARDS.

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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