RecruitingNot ApplicableNCT05494034
Yield of Implantable Cardiac Monitoring Device in Patients With Acute Ischemic Stroke.
Sponsor
National and Kapodistrian University of Athens
Enrollment
200 participants
Start Date
May 5, 2023
Study Type
INTERVENTIONAL
Conditions
Summary
In this prospective cohort study, the investigators aim to investigate the incidence of ICM-detected AF in unselected ischemic stroke patients and its association with anticoagulation initiation and stroke recurrence.
Eligibility
Min Age: 40 YearsMax Age: 100 Years
Inclusion Criteria4
- Consecutive acute ischemic stroke or TIA patients aged 40 years or older will be enrolled.
- Diagnosis of acute ischemic stroke will be based on clinical and neuroimaging evaluation \[brain computed tomography (CT) scan or magnetic resonance imaging (MRI) scan\].
- Stroke patients of all other etiologies (apart AF) presenting a HAVOC score ≥4 will be included in the study.
- Informed consent for participation in the study will be obtained from the patients or guardians of patients.
Exclusion Criteria2
- Patients with incomplete evaluation will be excluded, as previously described. \[22\] -Patients with known or newly detected AF at hospitalization will also be excluded.
- Not providing informed consent.
Interventions
DEVICEReveal LINQTM
implantable cardiac monitoring device ("Reveal LINQTM")
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT05494034
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