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Swiss Hemophilia Registry

S

Swiss Hemophilia Network

Status

Enrolling

Conditions

Hemophilia and Other Severe Bleeding Disorders

Treatments

Other: Registry

Study type

Observational

Funder types

Other

Identifiers

NCT02512250
2014-0667

Details and patient eligibility

About

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.

Enrollment

900 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

Diagnosis of hemophilia or other severe bleeding disorders. Signed inform consent

Exclusion criteria

None

Trial contacts and locations

19

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Central trial contact

Manuela Albisetti, MD

Data sourced from clinicaltrials.gov

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