Swiss Hemophilia Registry

NCT02512250 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 900

Last updated 2022-10-27

No results posted yet for this study

Summary

The Swiss Hemophilia Registry will collect data on the prophylactic and therapeutic use of factor concentrates in patients with hemophilia and other severe bleeding disorders in Switzerland.

Conditions

  • Hemophilia and Other Severe Bleeding Disorders

Interventions

OTHER

Registry

Sponsors & Collaborators

  • Swiss Hemophilia Network

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Switzerland

Study Locations

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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 NCT02512250 on ClinicalTrials.gov