The Severe Von Willebrand Disease (sVWD) Patient Registry

Recruiting Observational Study
VWD - Von Willebrand's Disease
No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Any
Study type
Observational
Participants needed
400 (estimated)
Sponsor
VWD Connect Foundation · Other
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About This Trial
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, labora…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Anyone meeting the diagnostic classification for von Willebrand disease 2. Any VWF antigen or activity: a. Result \<20% regardless of bleeding phenotype, or b. Result \<30% with excessive bleeding symptoms including: i. Bleeding that resulted in hospitalization, required …
Contacts

Christina Morgenthaler, MS, MBA

(279) 346-6202

morgenthaler@vwdregistry.org

CONTACT