About this trial
Currently, few recommendations exist for patients with mild hemophilia, who represent approximately 60% of the hemophilia population. This study aims to provide objective data on joint health in these patients, which are currently limited compared to those with moderate or severe hemophilia.
The use of joint ultrasound in mild hemophilia could allow early, asymptomatic detection of joint damage, support tailored management including patient education, and ultimately improve quality of life.
The study will also explore the correlation between coagulation factor levels (FVIII or FIX) and other indicators of joint health in France.
Eligibility criteria
Qualifiers
Adult (≥18 years old) with congenital mild hemophilia, defined as historical coagulation factor level >5% and <40% (FVIII or FIX).
Affiliated with a social security system.
Provided written informed consent to participate in the study.
Disqualifiers
Patient with acquired hemophilia.
Patient with uncontrolled chronic rheumatologic disease, such as rheumatoid arthritis, inflammatory spondyloarthropathies, or microcrystalline arthritis.
Known pregnancy or breastfeeding.
Patient deprived of liberty or under legal guardianship or conservatorship.
Trial design
Treatments tested in this trial
- Joint Ultrasound (HEAD-US)
- Blood Sample for Coagulation Factor Measurement
Treatment groups
Sponsors and collaborators
Assistance Publique - Hôpitaux de Paris
Lead sponsor
URC-CIC Paris Descartes Necker Cochin
Collaborator
Swedish Orphan Biovitrum
Collaborator