Can the Lambre Device Occlude IRRegular And Large Appendages in Patients With Non-Valvular AF

Launched by BRIAN O'NEILL MD · Dec 23, 2020

Keywords

ClinConnect Summary

This clinical trial is studying a device called the LAmbre Plus™ that is designed to help patients with a heart condition known as non-valvular atrial fibrillation (AF). People with AF have an increased risk of stroke because blood clots can form in a small pouch in the heart called the left atrial appendage (LAA). The goal of the trial is to see if using this device to close off the LAA is a safe and effective alternative to taking blood-thinning medications, which are often used to prevent strokes.

To be eligible for this trial, participants must be adults aged 18 or older who have been diagnosed with AF and are at a higher risk for stroke, indicated by specific scoring systems. They should also be suitable for short-term blood thinners but looking for a non-medication option. Some people may not qualify for the study, such as those who are pregnant, have certain heart conditions, or have recently had other medical procedures. Participants will receive the device and will be monitored over time to assess its effectiveness and safety. If you or a loved one is interested, it's important to discuss this trial with a healthcare provider to understand the potential benefits and risks.

Gender

ALL

Eligibility criteria

• Potential subjects must meet ALL of the following criteria to be eligible for inclusion in the study:
• Inclusion Criteria:
• • 1. The patient is a male or non-pregnant female ≥18 years of age
• • 2. The patient has documented paroxysmal, persistent, or permanent non-valvular atrial fibrillation or flutter
• • 3. The patient has a CHADS2 score ≥ 2 or a CHA2DS2-VASc score of ≥ 3, and is recommended for oral anticoagulation therapy
• • 4. The patient is deemed by their physician to be suitable for short-term OAC, but there is an appropriate rationale for seeking a non-pharmacologic alternative to oral anticoagulation
• • 5. The patient is deemed suitable for LAA closure in a shared decision model with a non-implanting physician
• • 6. The patient is willing and able to comply with protocol-specified treatment and follow-up evaluations
• • 7. The patient (or his or her legally authorized representative) has been informed of the nature of the study, agrees to its provisions, and has been provided written informed consent approved by the appropriate Institutional Review Board (IRB) or Ethics Committee (EC)
• Potential subjects will be excluded if ANY of the following conditions apply:
• Exclusion Criteria:
• • 1. Pregnant or nursing patients and those who plan pregnancy in the period up to 1 year following index procedure. Female patients of childbearing potential must have a negative pregnancy test done within 7 days prior to index procedure per site standard test
• • 2. Patients with atrial fibrillation that is defined by a single occurrence, or that is transient or reversible (e.g., secondary to CABG, an interventional procedure, pneumonia, or hyperthyroidism)
• • 3. Patients who require long-term anticoagulation/DAPT for a condition other than atrial fibrillation
• • 4. Patients not suitable for short term oral anti-coagulation (including due to bleeding diathesis or coagulopathy or absolute contraindication to OAC or DAPT ) or who will refuse transfusion
• • 5. Patients with rheumatic mitral valve disease, known severe aortic stenosis requiring surgical or percutaneous valve replacement, or existing mechanical valve prosthesis
• • 6. Active infection with bacteremia
• • 7. Known hypersensitivity or contraindication to aspirin, clopidogrel, heparin/bivalirudin, any device material or component (nitinol, nickel, titanium, PET), and/or contrast sensitivity that cannot be adequately pre-medicated
• • 8. Anatomic conditions that would prevent performance of the LAA occlusion procedure (e.g., prior atrial septal defect \[ASD\] or patient foramen ovale \[PFO\] surgical repair or implanted closure device, or obliterated left atrial appendage)
• • 9. Recent (within 30 days pre-procedure) or planned (within 60 days post procedure) cardiac or non-cardiac interventional or surgical procedure (e.g., cardioversion, ablation, percutaneous coronary intervention, cataract surgery, etc.)
• • 10. Recent (within 90 days pre-procedure) stroke, transient ischemic attack, or myocardial infarction
• • 11. Severe heart failure (New York Heart Association Class IV)
• • 12. Known asymptomatic carotid artery disease with\>70% diameter stenosis OR symptomatic carotid disease (\>50% diameter stenosis with ipsilateral stroke or TIA). Subjects with prior carotid endarterectomy or carotid stent placement may be enrolled, provided that known diameter stenosis is \<50%.
• • 13. Past or pending heart or any other organ transplant, or on the waiting list for any organ transplant
• • 14. Current participation in another investigational drug or device study
• • 15. Size of the left atrial appendage at the LAmbre Plus defined landing zone within outside the manufactures recommendations (Table 2.)
• • 16. Patients with an indication for chronic P2Y12 platelet inhibition therapy
• • 17. Patients who are unable to undergo CT scan
• • Echocardiographic Exclusion Criteria
• • 1. Left atrial appendage anatomy may accommodate implantation of the WATCHMAN device, according to IFU by size.
• • 2. LVEF \<25%
• • 3. Intracardiac thrombus or dense spontaneous echo contrast, as visualized by TEE within 2 days prior to implant
• • 4. Presence of a high-risk patent foramen ovale (PFO), defined as an atrial septal aneurysm (excursion \>15 mm or length \>15 mm) or large shunt (early, within 3 beats and/or substantial passage of bubbles)
• • 5. Moderate or severe mitral valve stenosis (mitral valve area \<1.5 cm2)
• • 6. Complex atheroma with mobile plaque of the descending aorta and/or aortic arch (Grade 4 or higher)
• • 7. Presence of an intracardiac tumor