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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04394195
Acronym
COVIDsFlt1
Enrollment
72
Registered
2020-05-19
Start date
2020-04-03
Completion date
2020-09-01
Last updated
2021-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CORONAVIRUS INFECTIONS

Brief 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.

Detailed 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.

Interventions

OTHERmeasurement of circulating sFlt1 concentration

blood circulating sFlt1 concentration will be determined

Sponsors

CHU de Reims
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Association between concentration of circulating sFlt1 and use of vasopressor14 days

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026