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A prospective multicenter study of the risk of developing CVD in hemophiliacs

A prospective multicenter study on risk assessment of cardiovascular diseases (CVD) in patients with hemophilia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1030240319
Enrollment
200
Registered
2024-09-05
Start date
2024-09-05
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemophilia A, Hemophilia B Acute Coronary Syndrome, Cerebral Infarction

Interventions

Performing non-contrast coronary CT imaging, non-contrast head and neck MRI imaging and pulse wave testing
D014057, D008279, D063177
coronary CT, head and neck MRI imaging,

Sponsors

Chikasawa Yushi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Congenital hemophilia A or hemophilia B (regardless of severity) Age of the patient must be at least 30 years old Informed consent is required

Exclusion criteria

Exclusion criteria: Acquired coagulation factor deficiency, including acquired hemophilia Congenital coagulation factor deficiency other than hemophilia Under 30 years of age. Unable to give informed consent Women who are pregnant or may become pregnant.

Design outcomes

Primary

MeasureTime frame
Framingham score, a risk score for cardiovascular disease Prevalence of coronary artery calcium score of 101 or higher on coronary CT PVH/DSWMH grade on head and neck MRI

Secondary

MeasureTime frame
Prevalence of those who are referred to a cardiologist or neurosurgeon specialist and require initiation of anticoagulation therapy

Contacts

Public ContactYushi Chikasawa

Tokyo medical university

yushi_c@tokyo-med.ac.jp+81-9052790786

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026