Association Between the Level of EV-TF and the Occurence of Pulmonary Embolism in Patients With ARDS

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Conditions studied: Acute Respiratory Distress Syndrome

In brief

In this study, 120 patients with Acute Respiratory Distress Syndrome (ARDS) will be included on a two years-period in an intensive care unit (Assistance Publique des Hôpitaux de Marseille, France). Those patients will benefit from a blood test at inclusion in order to measure several coagulation biomarkers, including EV-TF. Subsequently, these patients will be treated according to the usual practices of the department, following recommendations. Patients who received an injected CT scan between Day 5 and Day 28 will be divided into two groups based on the presence or absence of a pulmonary embolism on imaging. The measured values of EV-TF levels and other studied biomarkers will be compared between these two groups in order to detect a possible association between them and the diagnosis of pulmonary embolism. It should be noted that patients receiving an injected CT-scan between Day 5 and Day 7 will be included in the main analysis while those receiving it between Day 8 and Day 28 will be included in the secondary analysis. Others will be excluded from any analysis. At the same time, several collections of clinical data will be carried out: on Day 1, Day 7, Day 28, and on the day of the CT scan if it is performed at another time.

Key facts

Study ID: NCT05855317
Run by: Assistance Publique Hopitaux De Marseille
People needed: 170
Starts: 2023-10-31
Expected to finish: 2027-10-30
Last updated by the study team: 2026-02-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Patient 18 years of age or older,
Patient who has given his/her non-opposition to participate in this study, or alternatively, patient for whom a relative has given his/her non-opposition to participate in this study,
Patient admitted to intensive care for less than 24 hours,
Patient with ARDS according to the Berlin criteria,
Hypoxemia with PaO2/FiO2 ratio ≤ 300 on mechanical ventilation under PEEP ≥ 5 cmH2O,
Bilateral alveolar-interstitial opacities on chest imaging (chest X-ray or CT),
Exclusion of a cardiogenic cause on echocardiography,
Acute or subacute onset within 7 days based on the clinical-radiological profile.

You may not qualify if…

Positive SARS-CoV-2 PCR in a pharyngeal or respiratory sample (cytobacteriological examination of sputum, bronchial aspiration or bronchoalveolar lavage) prior to admission to the intensive care unit,
Patient with a pathology affecting the coagulation process or endothelial function (hemophilia, von Willebrand disease, etc.),
Patient receiving curative anticoagulant treatment before admission to the intensive care unit,
Patient undergoing extracorporeal veno-venous respiratory assistance (ECMO-VV) before admission to the intensive care unit,
Patient undergoing extra-renal purification with systemic anticoagulation with heparin before admission to the intensive care unit,
Persons referred to in articles L. 1121-5 to L. 1121-8 of the Public Health Code (minor patients, adult patients under tutorship or guardianship, patients deprived of their liberty, pregnant or nursing women),
Moribund patients for whom the life expectancy is less than 24 hours according to the opinion of the investigating physician.

Where it is running

Service Médecine intensive et réanimation — Marseille, France (enrolling)

Full record on ClinicalTrials.gov

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