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Study of Hemostasis in Case of Severe COVID-19

Study of Hemostasis in Case of Severe COVID-19

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04359992
Acronym
THROMBOVID
Enrollment
50
Registered
2020-04-24
Start date
2020-04-17
Completion date
2021-05-01
Last updated
2020-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19 Infection

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.

Interventions

OTHERExtra blood sample

3 extra blood samples at day 0, 2 and 7

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Platelet activation intensity with the occurrence of clinical thrombotic complicationsChange of platelet activity from admission's day in intensive care unit to 2 days and 7 days

Contacts

Primary ContactCharles TACQUARD
charlesambroise.tacquard@chru-strasbourg.fr369551608

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026