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Search / Trial NCT05627375

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

Deep Venous Thrombosis Pulmonary Embolism Anticoagulant Antiplatelet Venous Thromboembolism Direct Oral Anticoagulants Major Adverse Ischemic Cardiovascular And Cerebrovascular Event Secondary Prevention

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.

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

0 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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