Actively Recruiting
Thrombo Embolic Events in Hospitalized Patients With Covid-19 Serious Acute Pneumopathy
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-05-29
100
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the interaction between blood clotting and inflammation in patients hospitalized with COVID-19, especially those with severe pneumonia. This study aims to better understand how these processes contribute to the risk of blood clots in these patients. The project focuses on patients admitted to Amiens Hospital with COVID-19 infection to analyze their hemostasis and coagulation. The study involves collecting blood samples from patients at admission and weekly during their hospital stay to measure various blood clotting factors such as thrombin time, factor V, factor II, fibrin/fibrinogen degradation products, and antithrombin. Antibodies related to clotting disorders and SARS-CoV-2 viral load and immune response are also assessed at admission and four weeks later. In addition, venous ultrasound scans are performed weekly to check for blood clots until patients are discharged. Participants will undergo regular blood tests and ultrasound exams to monitor their blood clotting and inflammation status. Researchers will track changes in clotting factors and antibody levels over up to six weeks. The study measures include thrombin time, factor V and II concentrations, and fibrin degradation products. These assessments help understand the role of inflammation-induced thrombosis in COVID-19 patients. The total participation time depends on the hospital stay duration, with weekly monitoring until discharge.
CONDITIONS
Brief Title
Thrombo Embolic Events in Hospitalized Patients With Covid-19 Serious Acute Pneumopathy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- All patients hospitalized in Amiens Hospital with COVID-19 infection
You will not qualify if you...
- Patients younger than 18 years
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - From admission until discharge (up to 6 weeks)
Participants are monitored during their hospital stay with weekly venous ultrasound and blood samples for coagulation and hemostasis analysis.
Weekly visits during hospital stay
Trial Site Locations
Total: 1 location
1
CHU Amiens
Amiens, France, 80480
Actively Recruiting
Research Team
M
Michel Slama, Pr
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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