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Clinical Trials in France / NCT07450846
Recruiting Observational

Incidence and Evolution of Heart-lung Interaction in Acute Respiratory Distress Syndrome

NCT07450846 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2022-12-22
Last updated
2026-03-05

Condition(s) studied

Acute Respiratory Distress SyndromeRight Heart Failure

Study summary

Acute respiratory distress syndrome (ARDS) is an inflammatory injury of the lungs caused by various serious illnesses, such as a bacterial or viral lung infection. It is treated by artificial ventilation with the application of positive pressure. Pulmonary injury, coupled with artificial ventilation, can lead to right heart failure which hinders the ejection of blood to the pulmonary circulation. Modern mechanical ventilation modalities have reduced the frequency ("incidence") of this right heart failure in acute respiratory distress syndrome. A large-scale study has shown this a few years ago. However, the evolution of right heart failure during artificial ventilation, and the consequences it has on the patient's cardiovascular status are poorly determined. This study is conducted to improve knowledge in this area. In adult patients hospitalized in intensive care presenting acute respiratory distress syndrome, the investigators will collect the data recorded on cardiac ultrasound, doses of cardiovascular drugs as well as variables reflecting hemodynamic status and cell oxygenation. Data will be collected during the course of ARDS and mechanical ventilation, as well as after weaning from artificial ventilation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age ≥18 years old * Hospitalization in intensive care undergoing mechanical ventilation * Presence of ARDS according to the current consensus definition (Berlin definition) * Performance of at least one echocardiography during the first 24 hours of treatment, between the 2nd and 3rd day, between the 5th and 7th day, and within 48 hours of extubation Exclusion Criteria: Pregnancy Poor echogenicity preventing reliable measurement of the dimensions of the right and left ventricles.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chu de Bicêtre, AP-HP Le Kremlin-Bicêtre France Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07450846 on ClinicalTrials.gov ↗ ← All trials in France