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World Bleeding Disorders Registry

NCT03327779 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20000

Last updated 2023-08-14

No results posted yet for this study

Summary

The WBDR is an international observational disease registry of patients with hemophilia. It will provide a platform for a network of hemophilia treatment centres (HTCs) around the world to collect uniform and standardized patient data and guide clinical practice. With informed consent from the patient, the WBDR stores anonymous data about the person's disease, such as hemophilia type and severity, symptoms, and treatment.

Conditions

Sponsors & Collaborators

  • World Federation of Hemophilia

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-26
Primary Completion
2028-01-31
Completion
2028-01-31

Countries

  • Canada

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03327779 on ClinicalTrials.gov