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RECRUITINGINTERVENTIONAL

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

Prognosis Improvement of Unprovoked vEnous THromboEmbolism With the Use of a Shared Decision-making Process Including a Time-dependent Multicomponent Risk Prediction Scores inteRvention.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 months with full dose anticoagulant therapy, - Signed willing to sign a consent form. Who Should NOT Join This Trial: - Unable or refusal to give willing to sign a consent form, - 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) Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
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 months with full dose anticoagulant therapy, * Signed informed consent. 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)

Treatments Being Tested

OTHER

Usual Care Group

Patients will be managed as regards their anticoagulant treatment according to usual practice and in accordance with international guidelines.

OTHER

shared decision-making process

The intervention is based on a strategy based on a shared decision-making process which is a collaborative process that involves a patient and their healthcare professional working together to reach a joint decision about care (anticoagulant treatment). The shared decision-making process will be conducted as follows: * Step 1: prepare the risk estimates (risk of recurrent VTE, risk of bleeding) for the patient, based on time-dependent multicomponent risk prediction scores and socio-anthropological scales (TDMI) and other validated risk prediction scores and evidence-based medicine; * Step 2: Communicating risks, benefits and consequences to the patient; * Step 3: Make a joint decision about treatment and care, and agree together when this will be reviewed.

Locations (20)

CHU Brest
Brest, France, France
CHU d'Amiens - Picardie
Amiens, France
CHU d'Angers
Angers, France
Hôpital National d'Instruction des Armées Percy
Clamart, France
CHU de Clermont Ferrand
Clermont-Ferrand, France
APHP-Colombes
Colombes, France
CHU de Dijon - Hôpital François Mitterand
Dijon, France
CH Le Mans
Le Mans, France
HCL - Hôpital Edouard Herriot
Lyon, France
APHM - Hôpital la Timone
Marseille, France
CHU de Montpellier
Montpellier, France
CHU de Nancy
Nancy, France
CHU de Nantes
Nantes, France
CHU de Nîmes
Nîmes, France
Aphp-Hegp
Paris, France
Aphp-Hegp
Paris, France
CHU de Rennes
Rennes, France
CHU Saint Etienne
Saint-Etienne, France
CHU de Strasbourg
Strasbourg, France
CHU de Toulouse
Toulouse, France