Clin2
NCT05437536Possibly a fitRecruiting

Severe von Willebrand disease patient registry in the U.S.

VWD - Von Willebrand's Disease

Part of Blood & lymphatic, Genetic & congenital clinical trials.

This registry collects health and bleeding information from people who have severe von Willebrand disease (a lifelong bleeding condition). Your data helps researchers understand the condition better and supports future studies that may lead to better treatments.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
400 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a diagnosis of von Willebrand disease (from your doctor or your own confirmation).
  • You meet severe criteria based on VWF lab results (often very low), or you have significant bleeding problems.
  • You (or a legal representative) can give informed consent to join the registry.
  • You live in the United States.
  • You can follow study steps and share required information for data collection.
  • You do not have acquired von Willebrand disease (a type caused by another condition, not lifelong VWD).

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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