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INSU Cor Study: Insular – non Insular Stroke Underlying Cardiac failure

Recruiting
Conditions
I63
I64
I50
Cerebral infarction
Stroke, not specified as haemorrhage or infarction
Heart failure
Registration Number
DRKS00012454
Lead Sponsor
niversitätsklinikum WürzburgNeurologischen Klinik und Poliklinik
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
180
Inclusion Criteria

Ischemic stroke according to the WHO definition (Hatano 1976) or the corresponding lesion in cerebral imaging irrespective of the duration of the symptoms, maximum 3 days before inclusion with (cases) vs. without involvement (control) of the insular cortex
In screening by handheld or routine echocardiography free of systolic dysfunction
Written consent of the patient or written consent of the legal representative or relative is available
Sufficient German language skills

Exclusion Criteria

The exclusion criterion is the inclusion of the patient in an acute intervention / AMG study in order to monitor the natural course of cardiovascular diseases as well as comorbidities
Patients who were initially diagnosed with a stroke but who were subsequently diagnosed with a different diagnosis
Systolic dysfunction in screening
Lack of readiness / ability to perform follow-up appointments

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary endpoint is the development of new systolic dysfunction in ischemic cerebral infarction patients with involvement of the insular cortex within the first three months after index event.
Secondary Outcome Measures
NameTimeMethod
Identification of comorbidities (rehospitalisation rate, degree of independence, cognition, depression, anxiety) after 3 months, that are associated with development of a new systolic dysfunktion within the first three months after ischemic stroke<br>Cases and controls are compared by means of echocardiographic and clinical exams, blood based biomarkers, interviews about comorbidities, medication and risk factors after 1 week as well as 4 and 12 weeks.
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