Silent Stroke Clinical Trial
— SILENT2Official title:
Incidence of Silent Atrial Fibrillation in Patients With Clinically Silent Brain Ischemic Lesions (SILENT2)
NCT number | NCT04449523 |
Other study ID # | 2020-00227 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | September 8, 2020 |
Est. completion date | December 2025 |
Arterial Fibrillation (AF) is well-recognized as a cause for cryptogenic Acute Ischemic Stroke (AIS) and is associated with Silent Brain Infarction (SBI). However, the role of AF in the formation of lesions (SBIs) is less well established than its role in AIS and needs clarification. The investigators hypothesize that continuous rhythm monitoring will yield a similar incidence of AF diagnosis in patients with SBI as compared to patients with cryptogenic AIS. The primary objective is to assess the cumulative incidence of AF diagnosis at 24 months in patients with SBI.
Status | Recruiting |
Enrollment | 150 |
Est. completion date | December 2025 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 50 Years and older |
Eligibility | Inclusion Criteria: - Age - = 65 years - = 50 years AND one the following: - NT-proBNP >400 pg/mL - Left atrial ventricular index >42 ml/m2 or left atrial diameter >46 mm - Covert infarctions with cortical involvement in more than one vascular territory (left carotid territory, right carotid territory, vertebrobasilar territory) - Written informed Consent - Any clinically silent ischemic lesions of the brain parenchyma detected on neuroimaging defined according to established criteria as either: - Diffusion weighted imaging (DWI) positive lesions: Focus of restricted diffusion (high DWI signal and low apparent diffusion coefficient value) occurring in either white or gray matter, located in the cerebrum, cerebellum, or brain stem AND not satisfying the diagnostic criteria for multiple sclerosis OR - Cavitatory Lesions: = 3 mm in size that follow cerebro-spinal fluid on all sequences that are slit or wedge shaped with an irregular margin AND NOT longitudinally aligned with perforating vessels or with a multiple, bilateral symmetrical distribution OR - T2 weighted (T2W) hyperintense/T1 weighted (T1W) hypointense lesions: - Focal lesion with high T2W signal and low T1W signal that have prior evidence of restricted diffusion; OR - Present within cortical gray matter or deep gray matter nuclei OR - A lesion that is new, compared with an MRI performed within 3 months OR - T2W hyper/T1W hypointense lesions in the white matter, which are discontinuous but associated with the classic confluent periventricular T2 intense change of leukoaraiosis (Fazekas =2) AND NOT satisfying the diagnostic criteria for multiple sclerosis or with a significant patient history of severe trauma, radiation, drug toxicity, or carbon monoxide poisoning Exclusion Criteria: - History of AF or atrial flutter - Patients with a history of symptoms compatible with an AIS, covert neurological deficits are allowed. - Cardiac implantable electronic devices (pacemaker, implantable cardiac defibrillator (ICD), implantable cardiac monitor (ICM)) - Indication for cardiac implantable electronic device implantation (pacemaker, ICD, ICM) - History of or indication for major cardiac surgery or transcutaneous aortic valve implantation - Indication for permanent oral anticoagulation - Contraindication for permanent oral anticoagulation - Projected life expectancy of less than 2 years - Active intra- or extracranial high-grade malignancy - Patient is already included in another clinical trial that will affect the objectives of this study - Patient's lack of accountability, inability to appreciate the nature, meaning and consequences of the study and to formulate his/her own wishes correspondingly - Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. - Known or suspected non-compliance, drug or alcohol abuse |
Country | Name | City | State |
---|---|---|---|
Austria | Universitätsspital Graz | Graz | |
Germany | Charite Berlin | Berlin | |
Switzerland | Kantonsspital Aarau | Aarau | |
Switzerland | University Hospital Basel | Basel | |
Switzerland | Inselspital Bern | Bern | |
Switzerland | Centre hospitalier universitaire vaudois (CHUV) | Lausanne | Vaud |
Switzerland | Kantonsspital St.Gallen | Saint Gallen | |
Switzerland | Universitätsspital Zurich | Zurich |
Lead Sponsor | Collaborator |
---|---|
Insel Gruppe AG, University Hospital Bern |
Austria, Germany, Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Time to first diagnosis of AF (lasting =30 seconds; =6 minutes; =1 hour; = 24 hours) until battery depletion of Implantable Cardiac Monitor (ICM) (36-42 month). | From day 0 until battery depletion, expected to be 36 to 42 months | ||
Other | Cumulative incidence of AF diagnosis until battery depletion of ICM | From day 0 to until battery depletion, expected to be 36 to 42 months | ||
Primary | Cumulative incidence of Arterial Fibrillation (AF) diagnosis over a median of 24 months | Only adjudicated events will be used for the analysis. An AF episode is defined as lasting more than 30 seconds. A diagnosis of atrial flutter will also be considered as a primary endpoint. | From day 0 to 24 months after inclusion | |
Secondary | Time to first diagnosis of AF (lasting =30 seconds; =6 minutes; =1 hour; = 24 hour) | From day 0 to 24 months after inclusion | ||
Secondary | Burden of AF | The burden of AF is defined as the amount of time (percentage) in AF during rhythm monitoring. AF burden will be calculated on a monthly basis. | From day 0 to 24 months after inclusion | |
Secondary | Time to composite of first diagnosis of AF, stroke and death. | From day 0 to 24 months after inclusion | ||
Secondary | Incidence of AF diagnosis according to Silent Brain Infarction (SBI) neuroradiological appearance (subcortical small vessel versus embolic pattern involving grey matter) and SBI fulfilling ESUS criteria versus lacunar type. | Embolic stroke of undetermined source (ESUS) | From day 0 to 24 months after inclusion | |
Secondary | Start of oral anticoagulation therapy at 24 months. | At 24 months | ||
Secondary | Stroke at 24 months | At 24 months | ||
Secondary | Mortality at 24 months | At 24 months | ||
Secondary | Prevalence of other possible etiologies for SBI according to a modified TOAST-classification (large artery disease, small artery disease, other specific etiologies, unknown etiology, incomplete workup) | From day 0 to 24 months after inclusion | ||
Secondary | Incidence of new SBI at 24 months (only if sufficient funding can be obtained for repeat brain MRI at 24 months without contrast agent) | At 24 months |
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