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COMPLETED
NCT05074758

Characterization of the microVAScular Dysfunction in Covid-19 ARDS

Sponsor: Assistance Publique - Hôpitaux de Paris

View on ClinicalTrials.gov

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.

Official title: Characterization of the microVAScular Dysfunction in COvid-19 ARDS

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

39

Start Date

2021-12-10

Completion Date

2023-03-06

Last Updated

2026-07-08

Healthy Volunteers

No

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 )

Locations (1)

Hôpital européen Georges Pompidou

Paris, Paris, France