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Latin-American Von Willebrand Disease Registry

NCT04279717 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2020-02-21

No results posted yet for this study

Summary

Establish a Latin-American network of centers and professionals with the aim of:

* To register VWD patients in retrospective/prospective study, using a database, available online, common to all
* To register the bleeding history, the treatment and the events of VWD patients in the region
* To investigate the influence of VWD on quality of life

Conditions

  • Von Willebrand Disease

Interventions

OTHER

Observation

No interventions planned: treatment of patients at the discretion of the treating/responsible physician

OTHER

Observation

No interventions planned: treatment of patients at the discretion of the treating/responsible physician

Sponsors & Collaborators

  • Academia Nacional de Medicina

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-02-29
Primary Completion
2022-12-31
Completion
2022-12-31

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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 NCT04279717 on ClinicalTrials.gov