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A Database For The Collection Of Clinical, Laboratory, And Treatment Data From Patients With Factor X Deficiency To Define The Natural History Of The Disease And Improve Patient Management
Sponsor: Fondazione Luigi Villa
Summary
Factor X deficiency is one of the most severe rare bleeding disorders and may lead to serious spontaneous hemorrhages, particularly in patients with severe congenital forms. Acquired FX deficiency is even rarer, most frequently associated with AL amyloidosis, and remains poorly characterized. Establishing a comprehensive patient registry is essential to improve understanding of disease epidemiology, clinical manifestations, and treatment outcomes, ultimately supporting evidence-based management strategies.
Official title: Coagulation Factor X Deficiency: Natural History And Disease Management
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
20
Start Date
2026-06-14
Completion Date
2029-06-14
Last Updated
2026-10-15
Healthy Volunteers
Yes
Conditions
Locations (2)
Azienda Ospedaliero Universitaria Careggi. SODc Malattie Emorragiche e della Coagulazione
Florence, Italy
Angelo Bianchi Bonomi, Hemophilia and Thrombosis Center
Milan, Italy