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Standalone Thoracoscopic Left Atrial Appendage Closure Versus Medical Therapy in Atrial Fibrillation (STELLA-AF)

10 juli 2026 bijgewerkt door: Region Skane

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.

Studie Overzicht

Gedetailleerde beschrijving

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.

Studietype

Ingrijpend

Inschrijving (Geschat)

936

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Contact Back-up

Studie Locaties

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

  • Volwassen
  • Oudere volwassene

Accepteert gezonde vrijwilligers

Nee

Beschrijving

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

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Geen tussenkomst: Standard of care including best medical treatment
Standard of care including best medical treatment. This may include treatment with OAC, antiplatelet therapy and both or none of the above, depending on the characteristics of the patient and the clinical judgement of the responsible physician.
Experimenteel: Video-assisted thoracoscopic closure of the left atrial appendage using a closure device
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.
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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Number of participants strokes, major bleedings, other arterial thromboembolic events and cardiovascular or unknown death measured per 100 patient years.
Tijdsspanne: Mean follow up of 3 years
Intention 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.
Mean follow up of 3 years

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Analysis of risk ratio for primary endpoint
Tijdsspanne: Mean follow up of 3 years
As 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.
Mean follow up of 3 years
Proportion of patients receiving OAC treatment
Tijdsspanne: Mean follow up of 3 years
Mean follow up of 3 years
Quality of life survey; 36-Item Short Form Survey Instrument (SF-36)
Tijdsspanne: Baseline, 2 months after inclusion and 1 and 2 years after inclusion
Quality of life (QoL) measured using the 36-Item Short Form Survey Instrument (SF-36)
Baseline, 2 months after inclusion and 1 and 2 years after inclusion
Number of patients with need for catheter ablation
Tijdsspanne: Mean follow up of 3 years
Mean follow up of 3 years
Proportion of patients with need for new class I or III antiarrhythmic drugs for AF symptom reduction
Tijdsspanne: Mean follow up of 3 years
Mean follow up of 3 years
Procedural success
Tijdsspanne: Day 60 postoperatively
Procedural 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.
Day 60 postoperatively

Medewerkers en onderzoekers

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Sponsor

Publicaties en nuttige links

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Algemene publicaties

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Geschat)

1 januari 2028

Primaire voltooiing (Geschat)

31 december 2031

Studie voltooiing (Geschat)

31 december 2032

Studieregistratiedata

Eerst ingediend

6 juli 2026

Eerst ingediend dat voldeed aan de QC-criteria

10 juli 2026

Eerst geplaatst (Werkelijk)

15 juli 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

15 juli 2026

Laatste update ingediend die voldeed aan QC-criteria

10 juli 2026

Laatst geverifieerd

1 juli 2026

Meer informatie

Termen gerelateerd aan deze studie

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Ja

product vervaardigd in en geëxporteerd uit de V.S.

Ja

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