Appendage-Closing LAA Procedure Without Implants
Official title: Early Feasibility Study of the Append System for Left Atrial Appendage (LAA) Elimination by Invagination and Ligation in Prague
Run by Append Medical Ltd. · NCT07816029 · Data updated 2026-11-12
This procedure tests whether the Append System can safely close the left atrial appendage in adults with non-valvular atrial fibrillation.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 75 (estimated) |
| Sponsor | Append Medical Ltd. Industry-sponsored |
| Locations | 1 site (Prague) |
| Status | Recruiting |
| Started | July 16, 2025 |
| Main results expected | December 2027 |
| Study ends | June 2033 |
| Registry record updated | September 11, 2026 |
| Trial ID | NCT07816029 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with non-valvular AF and adequate CHA2DS2-VASc scores who are appropriate for LAA ligation and post-procedure anticoagulation/antiplatelet therapy.
✕Probably not a fit
Patients not achieving effective LAA closure or not tolerating the post-procedure medication regimen may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study evaluates the safety and performance of the Append System, which invaginates and ligates the left atrial appendage via a transfemoral, transseptal, transcatheter approach without a permanent implant. Patients with non-valvular AF who are candidates for LAA closure are enrolled and followed for up to 5 years to assess safety, device performance, and long-term outcomes. The trial focuses on feasibility, procedural success, and thromboembolism risk reduction related to LAA closure.
Why it matters
Potential benefit: If successful, the procedure could reduce stroke risk in AF patients without leaving a permanent implant in the heart.
How similar studies have gone: Previous approaches to LAA closure with implants have shown safety and efficacy, but this study explores a non-implant ligation method with newer feasibility data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Male or non-pregnant female aged ≥18 years 2. Documented non-valvular AF (paroxysmal, persistent, permanent or non-rheumatic valve-related AF) 3. The subject has a calculated CHA2DS2-VASc score of 2 or greater for males or 3 or greater for females. 4. The subject is eligible for the defined protocol medication regimen of anticoagulation and antiplatelet therapy following Append procedure. 5. The patient is deemed appropriate for LAA ligation by the screening committee and the investigator. 6. The patient has been informed of the nature of the study, agrees to its provisions \& follow-up evaluations, and has provided written informed consent approved by the appropriate Institutional Review Board (IRB) or Ethics Committee (EC). Exclusion Criteria: 1. Pregnant or nursing patients and those who plan pregnancy in the period up to 1 year following the index procedure. Female patients of childbearing potential must have a negative pregnancy test (per site standard test) within 7 days prior to index procedure. 2. Atrial fibrillation that is defined by a single occurrence or that is considered to be reversible (e.g., due to thyroid disorders, acute alcohol intoxication, trauma, or recent major surgical procedures). 3. Patients with an indication for chronic oral anticoagulation other than AF (e.g., history of unprovoked deep vein thrombosis or pulmonary embolism, or mechanical heart valve) 4. Clinically significant Severe heart failure (New York Heart Association functional class IV) 5. Prior cardiac surgery or surgery requiring sternotomy 6. Recent (within 3 months pre-procedure) stroke or transient ischemic attack. 7. Recent (within 3 months pre-procedure) myocardial infarction 8. Recent (within 30 days before the index procedure) or planned (within 60 days after the index procedure) cardiac interventional procedures (e.g., percutaneous coronary intervention, structural heart valve procedures, etc.), not including catheter ablation. 9. Planned (within 60 days after the index procedure) cardiac surgical procedures or any surgeries which require sternotomy. 10. Recent (within 30 days before the index procedure) or planned (within 60 days after the index procedure) noncardiac procedures or surgical interventions. 11. History of symptomatic pericarditis (acute or chronic). 12. Patient has evidence of cardiac tumor 13. Renal insufficiency, defined as estimated glomerular filtration rate (eGFR) \<30 mL/min/1.73 m2 (by the Modification of Diet in Renal Disease equation), or dialysis at the time of screening 14. Platelet count \<50,000 cells/mm3 or \>700,000 cells/mm3, or white blood cell count \<3,000 cells/mm3 or known Bleeding diathesis 15. Active infection with bacteremia 16. Patient has a known allergy, hypersensitivity or contraindication to aspirin, heparin, or that would preclude any P2Y12 inhibitor therapy, or the patient has contrast sensitivity that cannot be adequately pre-medicated 17. Current participation in another investigational drug or device study that would interfere with this study 18. Patient is unable to undergo general anesthesia 19. Patient has a condition which precludes adequate transesophageal echocardiographic (TEE) or computed tomographic (CT) assessment. 20. Known other medical illness or known history of substance abuse that may cause non-compliance with the specified medication regimen, confound the data interpretation, or is associated with a life expectancy of less than 5 years. Cardiac Imaging Exclusion Criteria 1. Intracardiac thrombus observed during screening 2. Left ventricular ejection fraction (LVEF) \<30% 3. Circumferential pericardial effusion \>5 mm or signs / symptoms of acute or chronic pericarditis, or evidence of tamponade physiology 4. Distance from inter-atrial septum fossa ovalis to LAA ostium is less than 40 mm 5. Any anatomy or prior intervention that would preclude a transseptal approach (including, but not limited to, prior IVC filter placement that cannot be crossed, prior ASD, or prior PFO closure device implantation that precludes transseptal puncture) 6. LAA structure that in the opinion of the screening committee / investigator precludes intervention
Where it's running
-
Charles University and Faculty Hospitals Motol and Homolka
Prague, Czechia Recruiting
Study contacts
- Study coordinator: Liz Zinger, MSc
- Email: liz.zinger@appendmedical.com
- Phone: (+972)-502071741
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Append System for closing the left atrial appendage
This study will test whether the Append System can safely close the left atrial appendage to lower stroke risk in adults with non-valvular atrial fibrillation.
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Assessing stroke risk in patients with newly diagnosed atrial fibrillation
This study is testing how to identify stroke risk in people who have just been diagnosed with atrial fibrillation to see who might need blood-thinning medication to prevent strokes.
-
Effects of anticoagulant interruption and left atrial occlusion in patients with bleeding from radiation cystitis and atrial fibrillation
This study looks at patients who have bleeding from radiation cystitis while on blood thinners for atrial fibrillation to see how these factors affect their treatment and outcomes.
-
Closure of the left atrial appendage to prevent embolic events in atrial fibrillation patients
This study is testing if a new device can safely close a part of the heart to help prevent blood clots in people with atrial fibrillation who have already had related health issues.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.