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Evaluation of Secondary Prevention of Stroke Study in the Outpatient Clinic

Evaluation of Secondary Prevention of Stroke Study in the Outpatient Clinic - ESPRESSO

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35302
Enrollment
200
Registered
2011-11-02
Start date
2011-12-12
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

cerebrovascular accident Stroke

Interventions

Standardized, regular check ups during one year after the initial event, performed at the SPC in our outpatient neurology department.

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age at least 18 years 2. Stroke (ischemic or haemorrhagic) 3. Visitor of the AMC outpatient clinic

Exclusion criteria

Exclusion criteria: 1. Stroke caused by subarachnoidal haemorrhage or cerebral venous sinus thrombosis 2. Dissection of the carotid artery (these patients have no cardiovascular risk factors for stroke recurrence) 3. No informed consent obtained

Design outcomes

Primary

MeasureTime frame
The primary outcome is a composite score on a newly proposed stroke-prevention-scale. This composite score will be calculated based on the presence or absence of the risk factors and the established relative risk (RR) as published in the literature.

Secondary

MeasureTime frame
1. Stroke caused by subarachnoidal haemorrhage or cerebral venous sinus thrombosis 2. Dissection of the carotid artery (these patients have no cardiovascular risk factors for stroke recurrence) 3. No informed consent obtained

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)