Thrombo Embolic Events in Hospitalized Patients With Covid-19 Serious Acute Pneumopathy

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire, Amiens

About this trial

The understanding of haemostasis and inflammation cross-talk has gained considerable knowledge during the past decade in the field of arterial and venous thrombosis. Complex and delicately balanced interaction between coagulation and inflammation involve all cellular and humoral components.

Elements of the coagulation system such as activated thrombin, fibrinogen or factor Xa may increase inflammation by promoting the production of proinflammatory cytokines, chemokines, growth factors and adhesion molecules that lead to a procoagulant state amplifying the pathological process. Recent evidence supports inflammation as a common pathogenic contributor to both arterial and venous thrombosis, giving rise to the concept of inflammation induced thrombosis.

Patients with infection of COVID-19 and severe pneumoniae seem to have higher risk of thromboembolism. The purpose of this project is to analyze hemostasis and coagulation of every hospitalized patient with infection of COVID-19.

Blood sample for coagulation and hemostasis analysis will be collected on every patient hospitalized in Amiens hospital for COVID-19 infection. Thrombin time, factors V and II, fibrin/fibrinogen degradation products, antithrombin will be assessed every week. Anticardiolipin, anti-beta2 glycoprotein I and anti-annexin A2 antibodies IgG and IgM at day of admission and at fourth week after admission will be assessed. SARS-CoV2 viral load and serodiagnosis will be performed at the same time. At the same time venous ultrasound to diagnose thrombosis will be performed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

all patients hospitalized in Amiens Hospital with COVID-19 infection

Disqualifiers

patients< 18 years

Trial population

Every patient hospitalized in CHU Amiens with COVID-19 infection

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • venous ultrasound

    Other intervention

    Venous ultrasound will be performed on patients once a week, every week from the day of admission in Amiens Hospital until the day of patient discharge

  • blood sample

    Biological/Vaccine

    blood sample for coagulation and hemostasis analysis will be withdrawn from artery catheter from the day of admission in Amiens Hospital until the day of patient discharge

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Variation of thrombin time (in secondes) in Hospitalized Covid-19 patients

Variation of thrombin time (in secondes) in Hospitalized Covid-19 patients. The reference range for the thrombin time is usually less than 20 seconds (ie, 15-19 seconds)

Time frame
up to 6 weeks
2

Variation of factor V concentration (U/dL) in Hospitalized Covid-19 patients.

Variation of factor V concentration (U/dL) in Hospitalized Covid-19 patients.

Time frame
up to 6 weeks
3

Variation of factor II concentration (U/dL) in Hospitalized Covid-19 patients

Variation of factor II concentration (U/dL) in Hospitalized Covid-19 patients

Time frame
up to 6 weeks
4

Variation of concentration of fibrin and fibrinogen degradation products (≥ 10 µgm/mL) in Hospitalized Covid-19 patients.

Variation of concentration of fibrin and fibrinogen degradation products (≥ 10 µgm/mL) in Hospitalized Covid-19 patients.

Time frame
up to 6 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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