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Standalone Thoracoscopic Left Atrial Appendage Closure Versus Medical Therapy in Atrial Fibrillation

Standalone Thoracoscopic Left Atrial Appendage Closure Versus Medical Therapy in Atrial Fibrillation

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07705282
Acronym
STELLA-AF
Enrollment
936
Registered
2026-07-15
Start date
2028-01-01
Completion date
2032-12-31
Last updated
2026-07-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ATRIAL APPENDAGE CLOSURE for ATRIAL FIBRILLATION, Oral Anticoagulation, Thoracotomy

Keywords

Left atrial appendage closure, Atrial fibrillation

Brief summary

Surgical left atrial appendage closure (LAAC) has been associated with reduced rates of stroke in patients with atrial fibrillation (AF) who have undergone cardiac surgery. In recent time, procedures with catheter-based devices for LAAC have failed to achieve results that would make them considered a safe alternative to oral anticoagulation. Several concerns regarding catheter-based devices have been raised due to their contact with circulating blood, device migration and periprocedural complications. LAAC using an externally placed clip via thoracoscopy would elude some of these concerns and may therefore be a feasible alternative to oral anticoagulation in patients with AF. This study aims to assess whether thoracoscopic left atrial appendage closure (TLAAC) is noninferior to medical treatment in patients with AF and an elevated bleeding risk using or being planned to initiate OAC and in those patients with clinical contraindications to oral anticoagulants.

Detailed description

Atrial fibrillation (AF) is the most common sustained arrhythmia worldwide and is associated with a markedly increased risk of ischemic stroke, heart failure, cognitive decline, systemic embolism, hospitalization, and mortality. AF-related strokes are often severe, disabling, and recurrent. Based on extrapolation of published regional Swedish data, 350-400 000 individuals in Sweden have atrial fibrillation, of whom 81% are treated with OAC:s. Despite major advances in anticoagulation, AF continues to represent one of the most important cardiovascular contributors to long-term disability and healthcare expenditure. For decades, oral anticoagulation with vitamin K antagonists represented the cornerstone of stroke prevention. The introduction of direct anticoagulant (DOAC) treatment fundamentally altered the therapeutic landscape. Trials including RE-LY, ROCKET-AF and ARISTOTLE demonstrated that DOAC therapy provides excellent protection against stroke/systemic embolism while reducing intracranial hemorrhage compared with warfarin. Consequently, DOACs became the standard of care for most patients with nonvalvular AF and are supported as first line treatment for most patients with nonvalvular AF. However, anticoagulation is not without its downsides. Despite modern OACs, treatment poses a significant bleeding risk and a lifelong treatment burden. Clinical decision making is complicated by patient frailty, renal dysfunction, liver disease and by patients with previous history of intracranial or gastrointestinal bleeding. Furthermore, long-term adherence is imperfect in real-world practice. In above mentioned trials, the annual bleeding risk ranged from 2.1-3.6% in patients treated with OAC, corresponding to 8400-14400 Swedish patients having major bleeding events from AF-related OAC treatment each year. Long-term anticoagulation may be associated with treatment burden, fear of bleeding, reduced treatment satisfaction, and impaired quality of life in some patients. Thus, the concept of a nonpharmacological strategy to prevent stroke remains highly attractive. Left atrial appendage closure While initial trials showed promising results of catheter based endocardial LAAC in the Warfarin era, the CLOSURE-AF trial recently showed that that endocardial devices, including the WATCHMAN™ and the Amplatzer™ Amulet™, do not achieve results making them a feasible replacement for modern OAC therapy in AF patients with elevated bleeding risk. The limitations of endocardial LAAC have several explanations. Implantation of a foreign body within the left atrium creates a potential substrate for thrombus formation. Device-related thrombi have been associated with increased risk of ischemic stroke and remain a recognized complication of endocardial LAAC. Incomplete sealing may allow persistent blood flow into the appendage, potentially preserving thromboembolic risk. In addition, many patients require OAC or dual antiplatelet therapy during the endothelialisation period. Procedure related risks include vascular complications, procedure-related stroke, device embolization and pericardial tamponade . The mechanistic rationale for left atrial appendage (LAA) exclusion originates from transoesophageal echocardiographic and autopsy studies demonstrating that the majority of intracardiac thrombi in nonvalvular AF arise from the LAA. The LAA is anatomically predisposed to thrombus formation because of reduced contractility, blood stasis, complex trabeculations, and impaired endothelial function during AF. This has led to the belief that mechanical elimination of the LAA may be a feasible alternative to systemic anticoagulation. Therefore, epicardial LAAC may be a feasible option to endocardial devices in AF patients with increased bleeding risk. The LAAOS III trial demonstrated that surgical LAAC was associated with a 33% risk reduction of stroke in patients undergoing cardiac surgery, and current guidelines recommend LAAC in patients with AF undergoing cardiac procedures. Thoracoscopic epicardial LAAC using devices including the AtriClip™ and Penditure™ may overcome several limitations of endocardial approaches. Firstly, no intracardiac foreign body is implanted, which reduces the risk of device-related thrombi. TLAAC requires no septal puncture and provides more complete anatomical exclusion of the appendage, with lower risk of residual leak. Cartledge and colleagues reported a series of 175 patients who underwent standalone TLAAC and demonstrated a 99.4% procedural success rate (defined as residual stump \<10mm) with low risk of procedural complications. One patient (0.6%) required conversion to sternotomy due to LAA bleeding. The cohort had a predicted annual stroke rate of 4.8% but no ischemic strokes were observed in study participants at a median follow up of 12.5 months, despite OACs being discontinued in 90.3% of patients at discharge. Furthermore, evidence suggests that the AF triggers located in the LAA may contribute to maintenance of AF itself. As the epicardial devices also create an electrical isolation, epicardial exclusion may therefore provide both thromboembolic and electrophysiological benefits.

Interventions

PROCEDUREVideo-assisted thoracoscopic closure of the left atrial appendage using a closure device and discontinuation of treatment if the patient is treated with OAC

Video-assisted thoracoscopic closure of the left atrial appendage using a closure device and discontinuation of treatment if the patient is treated with OAC. If indicated due to co-morbidities, patients will be prescribed platelet inhibitors instead.

Sponsors

Region Skane
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age ≥ 18 years and any of criteria 2-3 2. AF with a CHA2DS2-VA score ≥2 and a HAS-BLED score ≥3 or other clinically significant bleeding condition and ongoing OAC treatment 3. AF with a CHA2DS2-VA score ≥2 but deemed unfit for OAC by responsible physician due to clinical contraindications (e.g. amyloid angiopathy, previous intracranial haemorrhage or severe gastrointestinal bleeding).

Exclusion criteria

1. Clinical frailty score ≥5 2. Indication for OAC other than AF 3. Indication for dual antiplatelet therapy, if OAC is discontinued 4. Previous open-heart surgery 5. Present indication for cardiac surgery 6. Present indication for ablation for atrial fibrillation 7. Previous radiation therapy of the chest, due to malignancy 8. Previous pericarditis or myocarditis 9. Previous surgery including access to the left pleural space 10. Documented FEV1\<70% or other significant pulmonary disease (including but not restricted to fibrosis, pulmonary post-covid syndrome, cystic fibrosis) 11. Ongoing treatment with corticosteroids or previous treatment for more than 3 consecutive months. 12. Allergy to contrast media 13. Patient already included in another interventional clinical trial 14. Patient listed abroad, which would render them to be lost to follow-up after discharge 15. Patient does not understand study information given in the local language or, for other reasons, is deemed unfit to participate according to the investigators

Design outcomes

Primary

MeasureTime frameDescription
Number of participants strokes, major bleedings, other arterial thromboembolic events and cardiovascular or unknown death measured per 100 patient years.Mean follow up of 3 yearsIntention to treat analysis of the primary outcome is the composite endpoint of stroke, major bleeding defined as a BARC III bleeding, other arterial thromboembolic events and cardiovascular or unknown death measured per 100 patient years.

Secondary

MeasureTime frameDescription
Analysis of risk ratio for primary endpointMean follow up of 3 yearsAs treated analysis of the primary endpoint. Analysis of risk ratio for primary endpoint. Components of the composite endpoint per 100 patient years, analyzed separately. Procedural success defined as residual stump \<10mm using TOE intraoperatively and CT 60 days postoperatively. Healthcare cost-benefit analysis.
Proportion of patients receiving OAC treatmentMean follow up of 3 years
Quality of life survey; 36-Item Short Form Survey Instrument (SF-36)Baseline, 2 months after inclusion and 1 and 2 years after inclusionQuality of life (QoL) measured using the 36-Item Short Form Survey Instrument (SF-36)
Number of patients with need for catheter ablationMean follow up of 3 years
Proportion of patients with need for new class I or III antiarrhythmic drugs for AF symptom reductionMean follow up of 3 years
Procedural successDay 60 postoperativelyProcedural success will be verified with CT 60 days after the procedure and defined as no residual flow in the LAA and a residual stump length of \<10mm.

Countries

Sweden

Contacts

CONTACTIgor Zindovic, MD, Phd
igor.zindovic@skane.se+4646173300
CONTACTKarl Teurneau-Hermansson, MD, PhD
Karl.Teurneau-Hermansson@skane.se+4646173300

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 16, 2026