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Clinical Trials/NCT04359992
NCT04359992
Unknown
Not Applicable

Study of Hemostasis in Case of Severe COVID-19

University Hospital, Strasbourg, France0 sites50 target enrollmentApril 17, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19 Infection
Sponsor
University Hospital, Strasbourg, France
Enrollment
50
Primary Endpoint
Platelet activation intensity with the occurrence of clinical thrombotic complications
Last Updated
6 years ago

Overview

Brief Summary

The COVID-19 outbreak has led to a significant increase in the number of patients admitted to intensive care for respiratory distress. Early data indicate a particularly high risk of thrombotic risk to viral lung disease, particularly in the most severe patients, with a particularly high incidence of pulmonary embolism. Catheter thrombosis and extra-renal purification filters are also abnormally common. These thrombotic complications could contribute to the mortality observed in this pathology. The introduction of early curative anticoagulation in the most severe patients has just been proposed by the perioperative hemostasis interest group

Biologically, a significant proportion of patients hospitalized in intensive care have a marked biological inflammatory syndrome, associated with signs of activation of clotting (a frank increase in D-dimers). The presence of circulating anticoagulants is common. Interestingly, thrombocytosis, normally observed in such inflammatory syndromes, is absent.

In this context, it seems legitimate to explore these patients from a hemostasis perspective to identify the factors that cause this thrombotic over-risk, in order to minimize the occurrence of these complications.

Registry
clinicaltrials.gov
Start Date
April 17, 2020
End Date
May 1, 2021
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Strasbourg, France
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patient (\<18y)
  • With a SARS-CoV-2 infection confirmed by RT-PCR
  • Hospitalized in intensive care

Exclusion Criteria

  • Patients under guardianship/curator
  • Anemia at 7 g/dL at inclusion

Outcomes

Primary Outcomes

Platelet activation intensity with the occurrence of clinical thrombotic complications

Time Frame: Change of platelet activity from admission's day in intensive care unit to 2 days and 7 days

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