Best Antithrombotic Therapy in Patients With Acute Venous ThromboEmbolism While Taking Antiplatelets
Launched by CENTRE HOSPITALIER UNIVERSITAIRE DE SAINT ETIENNE · Nov 16, 2022
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial, titled "Best Antithrombotic Therapy in Patients With Acute Venous ThromboEmbolism While Taking Antiplatelets," is studying the best treatment options for patients who have both venous thromboembolism (VTE) and heart or blood vessel diseases. VTE includes conditions like deep vein thrombosis (DVT) and pulmonary embolism (PE), which can happen when blood clots form and block blood flow. The trial is looking at how well different combinations of blood-thinning medications can prevent further complications while managing the risks of side effects, like bleeding.
To participate in this trial, individuals need to be between the ages of 65 and 74, have a confirmed diagnosis of a recent DVT or PE, and be prescribed specific medications to prevent further heart and blood vessel issues. They also need to be able to provide informed consent and expect to live for more than three months. Participants can expect to receive careful monitoring and support throughout the study. It's important to know that the trial is currently recruiting, so there is an opportunity for eligible patients to contribute to important research that could improve treatment for others in the future.
Gender
ALL
Eligibility criteria
- • Inclusion criteria
- • Signed informed consent
- • Patients with acute objectively confirmed symptomatic proximal deep-vein thrombosis (DVT) or pulmonary embolism (PE) (with or without deep-vein thrombosis). Proximal deep-vein thrombosis is defined as thrombosis involving at least the popliteal vein or a more proximal vein of the lower limb.
- • Indication of full-dose anticoagulant therapy for at least 3 months.
- • Prescription of antiplatelet therapy for secondary prevention of atherosclerotic cardiovascular diseases, at the time of VTE diagnosis
- • Life expectancy more than 3 months
- • Social security affiliation
- Exclusion Criteria:
- • Unable to give informed consent
- • Active bleeding or a high risk of bleeding contraindicating anticoagulant treatment; a systolic blood pressure of more than 180 mm Hg or a diastolic blood pressure of more than 110 mm Hg
- • Anticoagulation for more than 5 days prior to randomization
- • Active pregnancy or expected pregnancy or no effective contraception
- • Isolated distal deep vein thrombosis
- • Antiplatelet therapy prescribed for primary prevention of cardiovascular disease
- • Indication to maintain a dual-antiplatelet therapy.
- • Triple positive antiphospholipid syndrome, with arterial thrombosis
- • Major cardiovascular and cerebrovascular event in the past 12 months for acute coronary syndrome, and in the past 6 months for cerebrovascular diseases and peripheral arterial diseases
About Centre Hospitalier Universitaire De Saint Etienne
The Centre Hospitalier Universitaire (CHU) de Saint-Étienne is a leading academic medical center in France, dedicated to advancing healthcare through innovative clinical research and high-quality patient care. With a robust infrastructure that supports a wide range of medical specialties, CHU de Saint-Étienne fosters collaboration between healthcare professionals, researchers, and academic institutions. The center is committed to conducting rigorous clinical trials that adhere to ethical standards and regulatory requirements, aiming to improve treatment outcomes and enhance the overall health of the community. Through its dedication to scientific excellence and patient-centered care, CHU de Saint-Étienne plays a pivotal role in the advancement of medical knowledge and the development of new therapeutic interventions.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Montpellier, , France
Tours, , France
Angers, , France
Amiens, , France
Rouen, , France
Angers, , France
Limoges, , France
Dijon, , France
Saint étienne, , France
Paris, , France
Lyon, , France
Montbrison, , France
Lyon, , France
Besançon, , France
Marseille, , France
Nice, , France
Brest, , France
Castelnau Le Lez, , France
Clermont Ferrand, , France
Firminy, , France
Grenoble, , France
Le Puy En Velay, , France
Nancy, , France
Nantes, , France
Paris, , France
Paris, , France
Strasbourg, , France
Toulon, , France
Toulouse, , France
Patients applied
Trial Officials
Laurent BERTOLETTI, MD PhD
Principal Investigator
CHU SAINT-ETIENNE
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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