Characterization of the microVAScular Dysfunction in Covid-19 ARDS
NCT05074758 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 40
Last updated 2022-01-19
Summary
The primary endpoint of this research is to establish that the alveolar dead space is significantly higher in patients with COVID-19 ARDS, compared to patients with non-COVID-19 ARDS.
Secondarily, the investigators want to establish the prognostic value of the alveolar-dead space (measured iteratively) in patients with COVID-19 and non-COVID-19 ARDS, to establish the respective influences of the biological parameters of endothelial damage, of the biological parameters of coagulopathy, of the parameters set on the artificial ventilator on the value of the alveolar dead space; in ARDS patients with COVID-19 and non-COVID-19 ARDS, to establish the prognostic value of the laboratory parameters of endothelial damage and coagulopathy in patients with COVID-19 and non-COVID-19 ARDS.
Conditions
- ARDS, Human
- COVID-19 Acute Respiratory Distress Syndrome
Interventions
- DIAGNOSTIC_TEST
-
alveolar dead-space quantification
measurement of alveolar dead-space based on volumetric capnography
- DIAGNOSTIC_TEST
-
Coagulation activation and impaired fibrinolysis explorations
blood sampling: * Fibrinolytic components * NETs components * Elastase-derived fragments of proteins of interest
- DIAGNOSTIC_TEST
-
Endothelial activation / endothelial senescence
circulating endothelial cells, E-selectin, endoglin, LVEF-A, LVEFR-2, Angiopoietin -1 and -2, cKit and SDF-1 Willebrand factor (activity, antigen, multimeric analysis )
Sponsors & Collaborators
-
National Research Agency, France
collaborator OTHER -
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Jean-Luc Diehl, PhD · AP-HP, Hôpital Européen Georges Pompidou, Paris
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-12-10
- Primary Completion
- 2022-09-10
- Completion
- 2022-09-10
Countries
- France
Study Locations
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