← Eichor
Study identifier: NCT05437536 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Severe Von Willebrand Disease (sVWD) Patient Registry

Condition: VWD - Von Willebrand's Disease  ·  Sponsor: VWD Connect Foundation

PhaseN/A
Planned participants400
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Christina Morgenthaler, MS, MBA  ·  (279) 346-6202  ·  morgenthaler@vwdregistry.org

Always discuss trial participation with your own doctor first.

Locations (1)

VWD Connect FoundationWellington, Florida, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05437536