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Optimal early recognition of persons at high risk of aneurysmal subarachnoid haemorrhage

Optimal early recognition of persons at high risk of aneurysmal subarachnoid haemorrhage - ERASE

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON55759
Enrollment
500
Registered
2017-02-01
Start date
2017-03-30
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Intracranial aneurysm

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Age between 20 and 70 years - At least one first degree relative with an unruptured intracranial aneurysm identified by MRA, CTA or conventional angiography

Exclusion criteria

Exclusion criteria: - People who do not speak Dutch well enough to give informed consent - Any first degree relative with an aneurysmal subarachnoid hemorrhage - A history of an aneurysmal subarachnoid hemorrhage and/or unruptured intracranial aneurysm - A history of polycystic kidney disease, Ehlers-Danlos, or fibromuscular dysplasia - Relative contraindication(s) for MRA, e.g. pregnancy, an internal metal device such as a pacemaker, or claustrophobia - A serious condition that would interfere with the treatment of an UIA, e.g. severe comorbidity or reduced life expectancy

Design outcomes

Primary

MeasureTime frame
Objective 1) - the prevalence of UIA in persons with >=1 FDR with an UIA Objective 2) - the prevalence of potential risk factors for UIA development in persons with >=1 FDR with an UIA Objective 3) - the prevalence of UIA in persons with >=1 FDR with an UIA

Secondary

MeasureTime frame
Objective 1) - costs of screening for and preventive treatment of UIA - clinical outcome after preventive treatment of an UIA identified with screening - decision model studying cost-effectiveness expressed in costs per QALY Objective 2) - prediction model of risk of UIA in persons with >=1 FDR with an UIA Objective 3) - correlation of imaging markers on 3T and 7T MRA and biopsy findings of the UIA wall

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)