Seeking people with a bleeding disorder such as Hemophilia or Von Willebrand Disease for a registry to collect health data to address the needs and challenges of people living with bleeding disorders.
Participants in this registry agree to share their health information and provide at least one blood sample to be tested for factors that may cause bleeding disorders and for infectious diseases.
What we're hoping for
This registry is collecting health information from children and adults with a blood disorder such as Hemophilia or Von Willebrand disease to prevent and reduce health complications.
ClinicalTrials.gov Identifier: Not Available