sFlt1: a Biomarker of Organ Dysfunction in Critically-ill Patients With COVID-19?

  • STATUS
    Recruiting
  • participants needed
    200
  • sponsor
    CHU de Reims
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Updated on 5 August 2020
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organ failure
covid-19

Summary

Short description of the protocol intended for the lay public. Include a brief statement of the study hypothesis (Limit : 5000 characters) The management of critically-ill patients with organ failure due to COVID-19 represents a major healthcare burden. While endothelial inflammation has been reported in these patients, the pathophysiological mechanisms remain incompletely elucidated.

Description

Extended description of the protocol, including more technical information (as compared to the Brief Summary) if desired. Do not include the entire protocol; do not duplicate information recorded in other data elements, such as eligibility criteria or outcome measures. (Limit : 32 000 characters)

The soluble fms-like tyrosine kinase 1 (SFlt1) is the soluble form of VEGF-A receptor 1 (VEGFR1). By linking VEGF-A with a high affinity, sFlt1 blocks the VEGF-A / VEFR1 axis and impairs endothelial homeostasis. Its production increases during inflammation. We hypothesize that sFlt1 is upregulated and correlates with endothelial dysfunction and outcomes in critically-ill patients with COVID-19.

Details
Condition Coronavirus Infection
Age 18years - 100years
Treatment measurement of circulating sFlt1 concentration
Clinical Study IdentifierNCT04394195
SponsorCHU de Reims
Last Modified on5 August 2020

Eligibility

 Yes No Not Sure

Inclusion Criteria

Patient with documented COVID-19 (positive PCR)
Hospitalized in University Hospital of Reims
Patient or family who have previously consented

Exclusion Criteria

Patient <18 yo
Patient not insured under the French social security
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