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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05074758
Other study ID # APHP210693
Secondary ID 2021-A01339-32
Status Recruiting
Phase
First received
Last updated
Start date December 10, 2021
Est. completion date September 10, 2022

Study information

Verified date January 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Josephine Braun, PhD
Phone 01 44 84 17 38
Email josephine.braun@aphp.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


Description:

Endothelial damage and coagulation activation at the lung microvascular level may play an important role in the physiopathology of the COVID-19 ARDS. The project aims to prospectively investigate both bedside pulmonary physiological markers and biological markers of coagulopathy and endothelial dysfunction in COVID-19 and non-COVID-19 ARDS patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date September 10, 2022
Est. primary completion date September 10, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age> 18 years old - Invasive mechanical ventilation in place for less than 48 hours - Severe or moderate ARDS (defined according to the Berlin classification) - Virological confirmation by PCR of SARS-CoV-2 infection (ARDS COVID-19) - Lack of virological confirmation by PCR of SARS-CoV-2 infection (ARDS not linked to COVID-19) - Patient information Exclusion Criteria: - Massive pulmonary embolism - Chronic respiratory failure under long-term oxygen therapy - Dying patient

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
alveolar dead-space quantification
measurement of alveolar dead-space based on volumetric capnography
Coagulation activation and impaired fibrinolysis explorations
blood sampling: Fibrinolytic components NETs components Elastase-derived fragments of proteins of interest
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

Country Name City State
France Hôpital européen Georges Pompidou Paris

Sponsors (2)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris National Research Agency, France

Country where clinical trial is conducted

France, 

References & Publications (2)

Ackermann M, Verleden SE, Kuehnel M, Haverich A, Welte T, Laenger F, Vanstapel A, Werlein C, Stark H, Tzankov A, Li WW, Li VW, Mentzer SJ, Jonigk D. Pulmonary Vascular Endothelialitis, Thrombosis, and Angiogenesis in Covid-19. N Engl J Med. 2020 Jul 9;383(2):120-128. doi: 10.1056/NEJMoa2015432. Epub 2020 May 21. — View Citation

Diehl JL, Peron N, Chocron R, Debuc B, Guerot E, Hauw-Berlemont C, Hermann B, Augy JL, Younan R, Novara A, Langlais J, Khider L, Gendron N, Goudot G, Fagon JF, Mirault T, Smadja DM. Respiratory mechanics and gas exchanges in the early course of COVID-19 ARDS: a hypothesis-generating study. Ann Intensive Care. 2020 Jul 16;10(1):95. doi: 10.1186/s13613-020-00716-1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Prognostic value of alveolar dead space Recording the exhaled CO2 curve (side-stream capnography method) and volume curve, as determined by the mechanical ventilator, and computing the signals with the arterial CO2 partial pressure, reflecting the partial pressure of CO2 in the alveoli participating in gas exchanges), determined on arterial blood gas (ABG) sampling. Up to 28 days
Secondary Prognostic value of the alveolar dead space (measured iteratively) To establish the link between alveolar dead-space values and Day 20 mortality 20 days
Secondary Prognostic value of the alveolar dead space (measured iteratively) To establish the link between alveolar dead-space values and Day 20 mortality and Day-28 invasive ventilator-free days. 28 days
Secondary Level of circulating endothelial cells To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of progenitor cells To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of circulating stem cells To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of endothelial proteomics To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of D-dimers To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of Willebrand Factor To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of components of the fibrinolytic system To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of fragments of plasminogen To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Level of the components of the NETs (Neutrophil Extracellular Traps) To describe the biological parameters of endothelial damage and prognostic value Up to 28 days
Secondary Survival rate 90 days
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