World Bleeding Disorders Registry (WBDR)

W

World Federation of Hemophilia

Status

Enrolling

Conditions

Von Willebrand Diseases
Hemophilia B
Hemophilia A

Study type

Observational

Funder types

Other

Identifiers

NCT03327779
WBDR

Details and patient eligibility

About

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.

Full description

The WBDR is a prospective, global registry of patients diagnosed with hemophilia A and B. Following the success of a pilot study, implementation of the full scale WBDR is underway. The goals are to enroll at least 200 HTCs from more than 50 countries, and at least 10,000 people with hemophilia, during the first five years, aiming for representation of patients from around the world and from all levels of access to care. Minimal criteria for participation of HTCs include access to reliable internet, human resources for data entry and commitment to long-term enrolment and follow-up of patients. The WBDR database is being developed through a collaboration between the WFH, Karolinska Institute and Health Solutions. By combining data from countries around the world, the WBDR will provide a large amount of real world data, on which researchers can address important scientific and clinical issues. The World Bleeding Disorders Registry (WBDR) is intended to fill existing gaps in knowledge by collecting real world data on the patient clinical experience around the globe.

Enrollment

20,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients of participating Hemophilia Treatment Centres with Hemophilia A or B, or von Willebrand Disease

Exclusion criteria

none

Trial contacts and locations

0

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Central trial contact

Emily Ayoub, Ph.D.; Donna Coffin, M.Sc.

Data sourced from clinicaltrials.gov

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