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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04544891
Other study ID # 2020PI120
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date March 1, 2022

Study information

Verified date March 2022
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Severe Acute Respiratory Syndrome-Corona Virus-2 infection results in a mild infection in most of the patients. However, 15-20% require hospitalization, and among them, 15-20% will develop acute respiratory failure, leading to their admission in Intensive Care Unit. There are no accepted predictive criteria for aggravation. Severe forms of Coronavirus induced disease-19 (COVID-19) are the consequence of endotheliopathy, and hyperinflammatory and pro-coagulant state. The Triggering Receptor Expressed on Myeloid cells-1 (TREM-1) is an immunoreceptor that acts as an amplifier of the inflammatory response. TREM-1 is expressed on myeloid and endothelial cells. Its activation leads to endothelial activation and damage, hyperinflammatory, and pro-coagulant state. TREM-1 activation is associated with poor outcome during septic shock and myocardial infarction. We here aim at investigating the relationship between TREM-1 pathway activation and clinical degradation and outcome of COVID-19 hospitalized patients.


Recruitment information / eligibility

Status Completed
Enrollment 830
Est. completion date March 1, 2022
Est. primary completion date March 1, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria Consecutive COVID-19 hospitalized patients for less than 3 days Exclusion Criteria: No consent Pregnancy protected populations

Study Design


Related Conditions & MeSH terms


Intervention

Other:
blood sampling
Blood will be collected every 3 days until Day 28, discharge, or death

Locations

Country Name City State
France CHRU Limoges Limoges
France Central hospital Nancy

Sponsors (3)

Lead Sponsor Collaborator
Central Hospital, Nancy, France Inotrem, University Hospital, Limoges

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary prognostic value of the TREM-1 pathway activation on clinical worsening day 28
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