CoviTrem1: TREM-1 Pathway Activation in COVID-19

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Completed
CT.gov ID
NCT04544891
Collaborator
University Hospital, Limoges (Other), Inotrem (Industry)
830
2
17
415
24.5

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: blood sampling

Study Design

Study Type:
Observational [Patient Registry]
Actual Enrollment :
830 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Prognostic Significance of the TREM-1 Pathway Activation in COVID-19
Actual Study Start Date :
Oct 1, 2020
Actual Primary Completion Date :
Mar 1, 2022
Actual Study Completion Date :
Mar 1, 2022

Outcome Measures

Primary Outcome Measures

  1. prognostic value of the TREM-1 pathway activation on clinical worsening [day 28]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All

Inclusion Criteria Consecutive COVID-19 hospitalized patients for less than 3 days

Exclusion Criteria:

No consent Pregnancy protected populations

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHRU Limoges Limoges France 87042
2 Central hospital Nancy France

Sponsors and Collaborators

  • Central Hospital, Nancy, France
  • University Hospital, Limoges
  • Inotrem

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gibot Sébastien, Pr, Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT04544891
Other Study ID Numbers:
  • 2020PI120
First Posted:
Sep 10, 2020
Last Update Posted:
Mar 22, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 22, 2022