Cardiovascular and Venous Thromboembolism Disease in Patients with Von Willebrand Disease in the French West

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Brest

About this trial

Due to increasing of life expectancy, patients with von Willebrand disease are exposed to age-related pathologies such as cancer or cardiovascular diseases. Management of thrombotic events is challenging given the inherent bleeding risk in von Willebrand disease. Few data are currently available in the literature.

The aim of the study is to describe the frequency and nature of arterial and venous thromboembolic events and atrial fibrillation in patients with von Willebrand disease in the West of France.

The investigators will perform a retrospective multicenter study conducted in the von Willebrand population of the French West. Von Willebrand adult patients followed in one of the French West medical centers participating in the study, who presented deep vein thrombosis, pulmonary embolism, ischemic stroke, transient ischemic attack, acute coronary syndrome, acute limb ischemia, atrial fibrillation, arteriopathy of the lower limbs, angina will be eligible.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Von Willebrand disease

Adult

Followed-up in a reference center of West of France (Caen, Brest, Nantes, Rennes, Le Mans, Angers)

Consented to be included in BERHLINGO database

Disqualifiers

- Expression of opposition

Acquired von Willebrand syndrome

Patients under legal protection

Minor

Trial population

Patients with von Willebrand disease followed in a reference center in the French West and who have consented to be included in the BERHLINGO database (Base d'Etude et de Recherche pour Les INvestigateurs en Hémostase du Grand-Ouest) with a medical history of deep vein thrombosis, pulmonary embolism, ischemic stroke, transient ischemic attack, acute coronary syndrome, acute limb ischemia, angina, obliterating arteriopathy of the lower limbs or atrial fibrillation.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

To describe the frequency of arterial and venous thromboembolic events and cardiac arrhythmia due to atrial fibrillation in patients with Willebrand disease in the Greater West.

Occurrence of a thromboembolic event validated by an adjudication committee

Time frame
12 months
2

To describe the nature of arterial and venous thromboembolic events and cardiac arrhythmia due to atrial fibrillation in patients with Willebrand disease in the Greater West.

Occurrence of a thromboembolic event validated by an adjudication committee

Time frame
12 months

Secondary outcomes

1

Identify potential risk factors

identify whether certain risk factors are more prevalent in the population than others

Time frame
12 months
2

Number of revascularisation procedures, anticoagulants and antiaggregants prescribed for these conditions

Prescription of anticoagulant and/or antiaggregant treatment

Time frame
12 months
3

Evaluate the nature of treatments prescribed for these pathologies: revascularisation procedures, anticoagulants and antiaggregants

Revascularisation procedure (endovascular or surgical)

Time frame
12 months
4

Evaluate the tolerance of these treatments

Occurrence of clinical haemorrhage

Time frame
12 months

Other outcomes

Sponsors and contacts

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