EMO-COVID: Hemostatic Profile in Patients Affected by COVID-19

Sponsor
ANNA FALANGA (Other)
Overall Status
Recruiting
CT.gov ID
NCT04595110
Collaborator
(none)
400
1
13.5
29.6

Study Details

Study Description

Brief Summary

Coronavirus disease-2019 (COVID-19), a viral respiratory illness caused by the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2), has been associated with the occurrence of cardiovascular adverse events including acute myocardial injury, acute heart failure, cardiac arrhythmias, and thromboembolic disease. These complications represent an important issue in COVID-19 patients accounting for the increased morbidity and mortality of this syndrome. According to a scoping review, venous thromboembolism and stroke occurred in approximately 20% and 3% of patients, respectively, with higher frequency observed in severely ill patients admitted to intensive care units. Despite the use of pharmacological thromboprophylaxis, the thrombotic risk still remained elevated in severe COVID-19 patients, and the optimal doses and timing of anticoagulation are not yet defined. The pathogenesis of COVID-19 associated thrombosis recognizes a prominent role of endothelial damage induced by both direct viral injury and an excessive and aberrant hyper-inflammatory host immune response associated to an increase in infection-related cytokines and chemokines. The occurrence of a hypercoagulable state in COVID-19 patients associated to a profound endothelial cell activation/dysfunction can result in the pathological phenomenon of immunothrombosis.

In this study, in a prospective cohort of consecutive COVID-19 hospitalized patients, an extensive characterization of the hemostatic alterations were performed, in order to: 1) clarify mechanisms underlying the coagulopathy in these patients; 2) how and to what extent the concomitant infection with SARS-CoV-2 affect this coagulopathy; and 3) identify biomarkers potentially predictive of disease outcome (i.e. any thrombotic recurrence and death).

Condition or Disease Intervention/Treatment Phase
  • Other: Observational study

Study Design

Study Type:
Observational
Anticipated Enrollment :
400 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Extensive Investigation of the Hemostatic Profile in a Prospective Cohort of Patients Affected by COVID-19
Actual Study Start Date :
Mar 25, 2020
Anticipated Primary Completion Date :
Apr 25, 2021
Anticipated Study Completion Date :
May 10, 2021

Outcome Measures

Primary Outcome Measures

  1. Incidence of mortality among enrolled COVID-19 patients [up to 6 months from the date of the enrollment]

    Identification of variables for prediction of mortality derived from review of clinical records. Samples collected from identified participants with COVID19 diagnosis will be assessed to determine thrombotic and inflammatory biomarkers able to prediction of mortality.

  2. Incidence of thrombosis among enrolled COVID patients [up to 12 months from the date of the enrollment]

    Identification of COVID-19 patients with evidence of thrombotic event derived from review of clinical records. Samples collected from identified participants with COVID19 diagnosis will be assessed to determine thrombotic and inflammatory biomarkers.

Secondary Outcome Measures

  1. Evaluation the role of enoxaparin in the management of Covid-19-associated coagulopathy [Samples collected from identified participants with COVID19 diagnosis will be assessed to determine the effect of thromboprophylaxis on thrombotic and inflammatory biomarkers]

    up to 12 months from the date of the enrollment

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age> 18 years

  • Adult patients admitted with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) positivity (by real time-PCR) from nasal swab or deep respiratory specimen or with clinical signs suggestive of SARS-Cov-2

  • Patients who have signed informed consent. If there is no possibility of obtaining informed consent for the clinical picture (eg adult patients sedated and curarized for acute respiratory failure and consequent mechanical ventilation), the patient's consent will be assumed until the contrary will be manifested.

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Papa Giovanni XXIII Hospital - S.I.M.T. Bergamo Italy 24127

Sponsors and Collaborators

  • ANNA FALANGA

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ANNA FALANGA, Principal Investigator, A.O. Ospedale Papa Giovanni XXIII
ClinicalTrials.gov Identifier:
NCT04595110
Other Study ID Numbers:
  • EMO-COVID-ASSTPG23
First Posted:
Oct 20, 2020
Last Update Posted:
Oct 20, 2020
Last Verified:
Oct 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by ANNA FALANGA, Principal Investigator, A.O. Ospedale Papa Giovanni XXIII
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 20, 2020