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NCT05773638Recruiting

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

Source: ClinicalTrials.gov · Last updated 6 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
21 Feb 2023
Start date
26 Dec 2021
Primary completion date
26 Dec 2026
Lead sponsor
University Hospital, Brest
NCT number
NCT05773638

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 26 Dec 2021 to the primary completion date, 26 Dec 2026
  • 6 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Acquired von Willebrand syndrome

Other

  • \- Expression of opposition
  • Patients under legal protection
  • Minor

Who the study is looking for

  • 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
  • Have presented a thrombotic and/or embolic event or cardiovascular disease including deep vein thrombosis, pulmonary embolism, ischemic stroke, transient ischemic attack, acute coronary syndrome, acute limb ischemia or angina or obliterating arteriopathy of the lower limbs, atrial fibrillation.
  • Have not expressed their opposition

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU d Angers
Coordinator of this site? Confirm its status
AngersFranceNot yet recruiting
CHU de Brest
Coordinator of this site? Confirm its status
BrestFranceRecruiting
CHU de CAEN
Coordinator of this site? Confirm its status
CaenFranceNot yet recruiting
CH Le Mans
Coordinator of this site? Confirm its status
Le MansFranceNot yet recruiting
CHU de Nantes
Coordinator of this site? Confirm its status
NantesFranceNot yet recruiting
CHU de Rennes
Coordinator of this site? Confirm its status
RennesFranceNot yet recruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.