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NCT Number: NCT05627375

Best Antithrombotic Therapy in Patients With Acute Venous ThromboEmbolism While Taking Antiplatelets

Venous thromboembolism (VTE) and atherosclerotic cardiovascular disease share common risk factors and frequently coexist in the same patients.

Their management requires use of antithrombotic agents: anticoagulant therapy (AC) for secondary prevention of VTE recurrence, antiplatelet (AP) for secondary prevention of major adverse ischemic cardiovascular and cerebrovascular event (MACCE) in patients with atherosclerotic cardiovascular disease (coronary artery disease, atherosclerotic cerebrovascular disease, lower extremity peripheral arterial disease).

Side effects of antithrombotic drugs are the 1st cause of emergency admission and hospitalization for an adverse drug reaction (mainly bleeding), and the combination of AC with AP strongly increases this risk.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

CHU Amiens, Amiens, France

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About this study

Up to one third of VTE patients receive concomitant AP therapy, with conflicting results on patient outcomes. Concomitant therapy (AC+AP) has been associated with a higher risk of bleeding (up to 3-fold) when aspirin was associated with vitamin-K antagonist (VKA) in a multicenter cohort study, or with direct oral anticoagulants (DOACs) for acute VTE in a post-hoc subgroup analysis. Conversely, patients with acute VTE in whom clinicians decided to maintain AC+AP were found to have an increased risk of MACCE without any higher risk of bleeding, in a multicenter registry. However, in most cases, the type (aspirin or another) and indication (primary versus secondary prevention) of AP was unknown, as was the duration of the combination AC+AP, and therefore these observational results may be confounded. Therefore, there is persistent equipoise regarding the benefit/risk of combining an antiplatelet therapy with anticoagulation in patients undergoing treatment for VTE, when there is a prior history of atherosclerotic cardiovascular disease. This may explain why clinical practice varies widely.

Considering the conflicting data about the risk of bleeding in patients on AP therapy for secondary prevention, who need to start full-dose anticoagulant therapy for acute VTE, a randomized trial comparing the two strategies, in patients with acute VTE and with history of stable atherosclerotic cardiovascular disease is needed and justified.

The investigators hypothesize that a strategy based on the prescription of a full-dose AC therapy alone will decrease the risk of bleeding, when compared to the the strategy of combined AP and full-dose AC therapies, and that this strategy will translate in a positive net clinical benefit (a composite of clinically relevant bleeding, recurrent venous thromboembolism, and major adverse ischemic cardiovascular and cerebrovascular events).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Full-dose anticoagulant therapy (AC)

Drug

Anticoagulant (AC) therapy: at the investigator's discretion in accordance with international recommendations for the management of DVT/PE

Antiplatelet therapy (AP)

Drug

Aspirin (at a daily dose ≤100 mg) or Clopidogrel (at a daily dose ≤75mg)

Primary outcomes

  1. Clinically relevant bleeding

    Time frame: end of the full-dose treatment period, up to 12 months

    Clinically relevant bleeding is composite of major bleeding events and clinically relevant non-major bleeding events).

Secondary outcomes

  1. Net clinical benefit

    Time frame: end of the full-dose AC treatment period, up to 12 months

    Net clinical benefit is defined by the composite of clinically relevant bleeding, recurrent venous thromboembolism, and major adverse ischemic cardiovascular and cerebrovascular events

  2. Clinically relevant non-major bleeding

    Time frame: end of the full-dose treatment period, up to 12 months

  3. Major bleeding events

    Time frame: end of the full-dose treatment period, up to 12 months

  4. recurrent venous thromboembolism

    Time frame: end of the full-dose treatment period, up to 12 months

    proximal deep venous thromboembolism and/or pulmonary embolism symptomatic or incidental, and including fatal-PE

  5. arterial events

    Time frame: end of the full-dose treatment period, up to 12 months

    major adverse cardiovascular and cerebrovascular events (nonfatal ischemic stroke, nonfatal myocardial infarction, acute lower limb ischemia, lower limb amputation or revascularization for vascular causes, cardiovascular deaths),

  6. venous thromboembolism (VTE) sequels

    Time frame: end of the full-dose treatment period, up to 12 months

    post-thrombotic syndrome (defined as a Villalta score up to 4) and post-PE syndrome (defined as the combination of a persistant dyspnea with a NYHA (New York Heart Association) scale more than I with residual vascular obstruction on lung scan

Study contacts

Contact information is provided by the study sponsor or research team.

Carine LABRUYERE

CONTACT

[email protected]

(0)477120469 ext. +33

Laurent BERTOLETTI, MD PhD

CONTACT

[email protected]

(0)477829121 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Saint Etienne

Other

Collaborators

  • Ministry of Health, France

Registry information

Acronym: BAT-VTE

Important dates

Study start
2023
Primary completion
2027
Study completion
2028
First posted
Nov 25, 2022
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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