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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00012454
Enrollment
180
Registered
2017-08-02
Start date
2017-10-19
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

I63 I64 I50

Interventions

Group 1: For stroke patients with and without involvement of the insular cortex blood-based biomarkers as well as interviews concerning cardiovascular and concomitant diseases, medication and risk fac

Sponsors

Universitätsklinikum WürzburgNeurologischen Klinik und Poliklinik
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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 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.

Countries

Germany

Contacts

Public ContactFelipe A Montellano

Institut für Klinische Epidemiologie und Biometrie Würzburg

Montellano_F@ukw.de0931 / 201 47329

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026