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RECRUITING
NCT07875478

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

View on ClinicalTrials.gov

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

Locations (2)

Azienda Ospedaliero Universitaria Careggi. SODc Malattie Emorragiche e della Coagulazione

Florence, Italy

Angelo Bianchi Bonomi, Hemophilia and Thrombosis Center

Milan, Italy