Actively Recruiting

All Genders
NCT05437536

The Severe Von Willebrand Disease (sVWD) Patient Registry

Led by VWD Connect Foundation · Updated on 2026-04-22

400

Participants Needed

1

Research Sites

520 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

A web-based registry will be created by the sponsor, VWD Connect Foundation (VCF), to collect data on patients with severe Von Willebrand Disease (sVWD). Data will be self-reported by patients and/or collected by registry personnel, as appropriate. The purpose of the sVWD Patient Registry is to create a database of well-characterized (with respect to demographics, medical history, symptoms, laboratory and genetic data, etc.) patients with sVWD for participation in retrospective and prospective research.

CONDITIONS

Official Title

The Severe Von Willebrand Disease (sVWD) Patient Registry

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Anyone meeting the diagnostic classification for von Willebrand disease
  • VWF antigen or activity less than 20% regardless of bleeding symptoms, or less than 30% with significant bleeding such as hospitalization, surgery, transfusion, large hemoglobin drop, or serious bleeding events
  • Provide informed consent by participant or legal representative
  • Willing and able to follow study procedures and provide data
  • Reside in the United States
Not Eligible

You will not qualify if you...

  • Have a clinical diagnosis of acquired Von Willebrand Disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

VWD Connect Foundation

Wellington, Florida, United States, 33414

Actively Recruiting

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Research Team

C

Christina Morgenthaler, MS, MBA

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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