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Multicenter registry on gene polymorphism in cerebrovascular disease

Multicenter registry on gene polymorphism in cerebrovascular disease - NCVC Genome Registry

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000050750
Enrollment
3000
Registered
2023-04-15
Start date
2017-05-26
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

Cerebrovascular disorders (cerebral infarction, transient ischemic attack, cerebral hemorrhage, asymptomatic extracranial/intracranial steno-occlusion, subarachnoid hemorrhage, cerebral arteriovenous malformation, dural arteriovenous fistula, venous sinus thrombosis, moyamoya disease, reversible cerebral vasospasm syndrome)

Interventions

None listed

Sponsors

National Cerebral and Cardiovascular Center
Lead Sponsor
Department of Neurology, Graduate School of Medicine, Mie University
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Aged 20 years or older Patients with cerebrovascular disease admitted to the institutes within 7 days from symptom onset or the last-known-well date Patients with the provision of written informed consent for RNF213 p.R4810K genotyping examination and a comprehensive consent form for the NCVC Biobank

Exclusion criteria

Exclusion criteria: Patients deemed by the physician to be ineligible for participation in this study.

Design outcomes

Primary

MeasureTime frame
Recurrence rate of ischemic events during the observation period

Secondary

MeasureTime frame
Incidence of bleeding events, all-cause mortality, and cardiovascular death during the observation period

Countries

Japan

Contacts

Public ContactTakeshi Yoshimoto

National Cerebral and Cardiovascular Center Department of Neurology

yoshimototakeshi1982@ncvc.go.jp0661701070

Outcome results

None listed

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