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Recruiting NCT05631756

Correlation Between PaO2/FiO2 and Lung Ultrasound Score in the Intensive Care Unit

Trial Parameters

Condition Interstitial Lung Disease
Sponsor Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Study Type INTERVENTIONAL
Phase N/A
Enrollment 86
Sex ALL
Min Age 17 Years
Max Age N/A
Start Date 2023-01-26
Completion 2024-11-30
Interventions
Lung Ultrasound

Brief Summary

The goal of this physiological interventional prospective study is to evaluate the improvement of the previously demonstrated correlation between PaO2/ FiO2 and Lung Ultrasound score (LUSS) in patients admitted in the ICU with an intesrtitial syndrom (IS) on the ultrasound of all aetiologies at inclusion and at twenty four and forty eight hours. The main question it aims to answer is if the LUSS is a valid tool to evaluate the severity of the IS Participants will initially have an arterial blood gas to evaluate the PaO2/FiO2 and in the ten minutes a lung ultrasound to evaluate the LUSS. This will be repeated at twenty four and forty eight hours.

Eligibility Criteria

Inclusion Criteria: \- consent -\>17 years old Exclusion Criteria: * LUSS \< 2 Non Inclusion Criteria: * Patient with pathologies leading to chronic IS * Chronic Obstructive Pulmonary Disease (COPD) or active asthma * Patients under veino-veinous or veino-arterial " Extracorporeal Membrane Oxygenation " (ECMO) * Severe trauma patients * Less than twenty-four hours post operative patients * LUS not feasible: prone position, pneumonectomy history, severe obesity

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