VExUS in Ards Patients and Association with AKI
A single-center prospective observational study will be conducted with the aim of determining the prevalence of venous congestion during ARDS using venous Doppler and the VExUS score.
| Condition(s) | Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS) |
|---|---|
| Status | Recruiting |
| Study type | Observational |
| Summary | A single-center prospective observational study will be conducted with the aim of determining the prevalence of venous congestion during ARDS using venous Doppler and the VExUS score. |
| Who can participate | Inclusion Criteria: * Patients ≥18 years old * Moderate to severe ARDS according to the Berlin definition * Requiring catecholamine support * Undergoing invasive mechanical ventilation for less than 48 hours Exclusion Criteria: * Patients presenting with acute kidney injury KDIGO III requiring renal replacement therapy before the initial ultrasound evaluation * Requirement for veno-venous or veno-arterial ECMO circulatory support before inclusion * Patients with end-stage chronic kidney disease, on dialysis, and/or kidney transplant recipients * History of Child C cirrhosis and/or liver transplantation and/or portal hypertension * History of portal thrombosis * Known history of pulmonary hypertension * Pregnant women * Patients under legal protection * Patients who have expressed oppositio |
| Ages | 18 Years to 100 Years |
| Sex | All |
| Lead sponsor | Assistance Publique - Hôpitaux de Paris |
| Locations | Créteil, Val de Marne, France |
| Start date | 2024-12-02 |
| NCT ID | NCT06805409 |
| Official listing | https://clinicaltrials.gov/study/NCT06805409 |