The Severe Von Willebrand Disease (sVWD) Patient Registry

Recruiting now

Conditions studied: VWD - Von Willebrand's Disease

In brief

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.

Key facts

Study ID
NCT05437536
Run by
VWD Connect Foundation
People needed
400
Starts
2021-12-10
Expected to finish
2031-12-01
Last updated by the study team
2026-04-22

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.