Evaluation of Secondary Prevention of Stroke Study in the Outpatient Clinic

Completed

• Conditions: cerebrovascular accident; 10007963; Stroke

• Registration Number: NL-OMON35302
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

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

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

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary outcome is a composite score on a newly proposed<br /><br>stroke-prevention-scale. This composite score will be calculated based on the<br /><br>presence or absence of the risk factors and the established relative risk (RR)<br /><br>as published in the literature. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>1. Stroke caused by subarachnoidal haemorrhage or cerebral venous sinus<br /><br>thrombosis<br /><br>2. Dissection of the carotid artery (these patients have no cardiovascular risk<br /><br>factors for stroke recurrence)<br /><br>3. No informed consent obtained</p><br>