Shared Decision-making Process for Unprovoked vEnous THromboEmbolism Management. (ETHER )

Last updated: May 6, 2025
Sponsor: University Hospital, Brest
Overall Status: Active - Recruiting

Phase

N/A

Condition

Venous Thromboembolism

Venous Thrombosis

Blood Clots

Treatment

Usual Care Group

shared decision-making process

Clinical Study ID

NCT06731244
29BRC23.0189
2024-A01652-45
  • Ages > 18
  • All Genders

Study Summary

Venous thromboembolism (VTE) including deep vein thrombosis (DVT) and pulmonary embolism (PE) is a frequent disease and the third most common cause of cardiovascular death in the world after myocardial infarction and stroke. Anticoagulant therapy drastically reduces the risk of early VTE recurrence and death, but it exposes patients to a substantial risk of bleeding. Hence, determining the optimal duration of anticoagulant treatment for VTE is a major public health issue.

When major transient risk factors for VTE are identified (major surgery, immobilization...), patients generally do not need to extend anticoagulation beyond 3 months, whereas for VTE diagnosed in the context of cancer, therapeutic anticoagulation is required for as long as the cancer is considered "active".

However, in more than 50% of cases, venous thromboembolic disease occurs spontaneously, i.e. without any significant clinically detectable circumstance (known as unprovoked venous thromboembolic disease). In such patients, the risk of recurrence is high (35% recurrence rate at 5 years, with a 10% risk of death per recurrence). Scientific societies therefore recommend continuing anticoagulant treatment "indefinitely" (i.e. without programming a stop date or long-term treatment). However, this practice exposes these patients to an ongoing, non-negligible increase in the risk of bleeding, which could ultimately exceed the risk of recurrence of venous thrombo-embolic disease.

Optimizing anticoagulant therapy beyond the first three to six months of treatment is therefore a crucial and challenging issue, which could improve the long-term prognosis of patients with unprovoked thromboembolic venous disease.

Based on the quantitative and qualitative approaches implemented in MORPHEUS project granted by European Commission (HORIZON-HLTH-2022-TOOL-11-01 call), the investigators have combined predictive personalized medicine, through the use of risk biomarkers, with a patient-centered model of medicine, which, while based on an understanding of the patient's experience, leading to develop Time-Dependent Multicomponent risk prediction scores and socIo-anthropological scales (TDMI) integrated in a shared decision-making process regarding anticoagulant treatment duration in patients with a first episode of unprovoked VTE.

The aim of this study is to demonstrate that this strategy, based on a medical decision-making process shared between patients and physicians and including TDMI, reduces the risk of recurrence of thromboembolic venous disease (fatal or non-fatal), the risk of bleeding and all-cause mortality, and is associated with greater patient satisfaction after a first episode of unprovoked thromboembolic venous disease.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patient > or = 18 years,

  • Patient with a first episode of symptomatic unprovoked pulmonary embolism (PE)and/or proximal deep vein thrombosis (DVT) treated for 3 to 6 uninterrupted monthswith full dose anticoagulant therapy,

  • Signed informed consent.

Exclusion

Exclusion Criteria:

  • Unable or refusal to give informed consent,

  • Isolated distal DVT,

  • Isolated sub-segmental PE

  • Previous unprovoked VTE

  • Known CTEPH

  • Indication for anticoagulation other than DVT or PE (e.g.; atrial fibrillation,mechanic valves...),

  • Interruption of anticoagulation for 14 days or more before the inclusion,

  • Active cancer of less than 24 months,

  • Current pregnancy,

  • Life expectancy <18 months (e.g.; patients with an end-stage chronic disease)

  • Not affiliated to national insurance, social security (only for France)

Study Design

Total Participants: 2400
Treatment Group(s): 2
Primary Treatment: Usual Care Group
Phase:
Study Start date:
March 26, 2025
Estimated Completion Date:
October 31, 2028

Connect with a study center

  • CHU d'Amiens - Picardie

    Amiens, 80054
    France

    Site Not Available

  • CHU d'Angers

    Angers, 49933
    France

    Site Not Available

  • CHU Brest

    Brest, 29609
    France

    Active - Recruiting

  • Hôpital National d'Instruction des Armées Percy

    Clamart, 92140
    France

    Site Not Available

  • CHU de Clermont Ferrand

    Clermont Ferrand, 63000
    France

    Site Not Available

  • APHP-Colombes

    Colombes, 92700
    France

    Site Not Available

  • CHU de Dijon - Hôpital François Mitterand

    Dijon, 21079
    France

    Site Not Available

  • CH Le Mans

    Le Mans, 72037
    France

    Site Not Available

  • HCL - Hôpital Edouard Herriot

    Lyon, 69003
    France

    Site Not Available

  • APHM - Hôpital la Timone

    Marseille, 13005
    France

    Site Not Available

  • CHU de Montpellier

    Montpellier, 34295
    France

    Site Not Available

  • CHU de Nancy

    Nancy, 54511
    France

    Site Not Available

  • CHU de Nantes

    Nantes, 44093
    France

    Site Not Available

  • CHU de Nîmes

    Nîmes, 30029
    France

    Site Not Available

  • Aphp-Hegp

    Paris, 75015
    France

    Site Not Available

  • CHU de Rennes

    Rennes, 35200
    France

    Site Not Available

  • CHU Saint Etienne

    Saint Etienne, 42270 Saint Priest En Jarez
    France

    Site Not Available

  • CHU de Strasbourg

    Strasbourg, 67091
    France

    Site Not Available

  • CHU de Toulouse

    Toulouse, 31000
    France

    Site Not Available

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