Carotid Implants for PreveNtion of STrokE ReCurrEnce From Large Vessel Occlusion in Atrial Fibrillation Patients Treated With Oral Anticoagulation

What this study is about

Patients with atrial fibrillation (AF) who have had a prior stroke are at very high risk of recurrent ischemic stroke. About 40% of these strokes are due to large emboli which result in large cerebral vessel occlusion (LVO). This randomized control trial aims to address this unmet need by testing whether use of bilateral carotid filter implants in addition to OAC will reduce the risk of stroke in AF patients with recent (e.g. within 12 months) ischemic stroke vs. only OAC.

Who can join (things the study team will check)

✅ You may be able to join if…

• Documented history of clinical AF
• History of ischemic (i.e. non-hemorrhagic) stroke including symptoms of stroke resolving within 24 hours with positive neuro-imaging, meeting one of the following criteria: Group 1: Patient was on OAC at time of index stroke, with index stroke occurring < 6 week from enrollment Group 2: Patient was not on OAC at time of stroke, with index stroke occurring < 6 weeks from enrollment Group 3: Patient was on OAC at time of index stroke, with index stroke occurring 6 to 52 weeks from enrollment
• Planned use of a Vitamin K antagonist (VKA) or a direct oral anticoagulant (DOAC) for the duration of the trial
• Patient able to tolerate single antiplatelet therapy in addition to oral anticoagulation for 6 months, in the opinion of the investigator
• Bilateral ultrasound or angiogram demonstrating all of the following: i. For ultrasound, calculate the percentage of carotid stenosis using the Society of Radiologists in Ultrasound Consensus Criteria for Carotid Stenosis, where ≥50% stenosis is defined by internal carotid artery peak systolic velocity of ≥125 cm/sec, internal/common carotid peak systolic velocity ratio of 2 or more and end diastolic velocity of ≥40 cm/sec, or evidence of near occlusion. ii. For angiography, calculate the percentage of carotid stenosis using the North American Symptomatic Carotid Endarterectomy Trial (NASCET) criteria ([D - N]/D x 100, where N is the luminal diameter at the site of maximal narrowing and D is the diameter of normal distal internal carotid artery beyond the bulb where the artery walls are parallel.
  • Inner common carotid artery diameter range: ≥5.3 mm and ≤8.8 mm
  • Accessibility: up to 40 mm from skin to common carotid artery center
  • Implantation segment free of any atherosclerotic disease
  • Absence of carotid dissection or pre-existing stent(s) in common carotid artery
  • Absence of ≥50% stenosis of the internal carotid arteries as seen on ultrasound or angiography (CTA, MRA or DSA)
• Provision of informed consent

🚫 You may not be able to join if…

• Contraindication to oral anticoagulation (e.g. history of intracranial hemorrhage, known hereditary or acquired coagulation disorders, or recurrent major bleeding)
• Contraindication to additional single antiplatelet therapy for 6 months from randomization
• Previously documented 50% or greater stenosis, or high-risk plaque in the opinion of the investigator, of the common carotid, internal carotid, subclavian, vertebral, or intracranial arteries that has not been treated with a revascularization procedure (i.e. stent or angioplasty)
• Visualized active (acute/subacute) cervical or intracranial arterial thrombus (i.e. free-floating) on computed tomography (CT), magnetic resonance (MR), or digital subtraction (DS) angiography that is at risk of causing additional stroke/brain injury
• Previously documented aneurysm of the internal carotid artery or its branches (i.e. ophthalmic, posterior communicating, anterior choroidal, anterior cerebral and middle cerebral arteries) that is 6 mm or greater in diameter.
• Prior surgery or radiation of the neck at the implantation segment
• Pre-existing percutaneous left atrial appendage occlusion device that was implanted after most recent ischemic stroke
• Planned left atrial appendage occlusion procedure
• Female who is pregnant or non-postmenopausal female who is not willing to use an effective method of birth control during duration of the trial
• Overt systemic infection
• Known sensitivity to nickel or titanium metals, or their alloys
• Active participation in another investigational drug or device treatment trial
• Any other condition that in the opinion of the investigator may adversely affect the safety of the patient or would limit the patient's ability to complete the trial

Where this trial is running

• Mercyhealth Javon Bea Hospital - Riverside, Rockford, Illinois, United States
• Weill Cornell Medical Center, New York, New York, United States
• Erlanger Medical Center, Chattanooga, Tennessee, United States
• Methodist University Hospital, Memphis, Tennessee, United States
• Baptist Memorial Hospital-Memphis, Memphis, Tennessee, United States
• Hamilton General Hospital, Hamilton, Canada, Canada
• University Hospital, London, Ontario, Canada

Who to contact

Sagit Broder, MSc · +972587112116 · sagit@javelinmed.com

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT05723926.