Actively Recruiting
Cohort for Monitoring Patients With Venous Thromboembolic Disease
Led by University Hospital, Rouen · Updated on 2025-06-11
2000
Participants Needed
1
Research Sites
654 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Venous thromboembolic disease is a common pathology in the general population (1.5/1000), the prognosis of which depends in particular on the risk of recurrence. This risk depends essentially on whether the thrombotic episode was provoked or not. Thus, patients who present a thromboembolic event without any contributing factor have a high risk of recurrence, which encourages clinicians to continue anticoagulant treatment for a long time. However, anticoagulant treatment is the leading cause of hospitalization for iatrogenic causes and the leading cause of iatrogenic mortality. The benefit-risk balance of treatment must be evaluated regularly, which requires a good knowledge of the risk factors for thrombotic recurrence and the risk factors for hemorrhage.
CONDITIONS
Official Title
Cohort for Monitoring Patients With Venous Thromboembolic Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Experienced at least one venous thromboembolic episode such as deep vein thrombosis confirmed by Doppler ultrasound or CT venography
- Experienced pulmonary embolism confirmed by CT angiography, ventilation/perfusion scan, or confirmed deep vein thrombosis with respiratory signs consistent with pulmonary embolism
- Hospitalized in the Internal Medicine Department
- Seen by an Internal Medicine physician
- Case presented at the multidisciplinary thrombosis meeting
You will not qualify if you...
- Thrombosis that does not meet inclusion criteria, including cerebral venous thrombosis and mesenteric thrombosis
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Hospital of Rouen
Rouen, France, 76031
Actively Recruiting
Research Team
D
David DM MALLET, Director
CONTACT
V
Vincent VF FERRANTI, ARC
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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