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Ischemic StrokeELAPSENCT05976685

Early Closure of Left Atrial Appendage for Patients With Atrial Fibrillation and Ischemic Stroke Despite Anticoagulation Therapy

A study testing Left atrial appendage Occlusion and DOAC in people with Ischemic Stroke and Atrial Fibrillation, run by Insel Gruppe AG, University Hospital Bern at 34 sites in 6 countries.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
Search all trials

Trial summary

Atrial fibrillation (AF) is one of the most common cardiac arrhythmias and cardioembolic stroke due to AF is its major complication. Direct oral anticoagulants (DOAC) reduce the risk of cardioembolism in patients with AF. Despite DOAC therapy, there is a significant residual stroke risk of 1-2%/year. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Ischemic Stroke, Atrial Fibrillation
What is being tested?
Left atrial appendage Occlusion and DOAC
Could I receive a placebo?
No, everyone receives an active treatment
How many people
482 participants
Where
34 sitesin 6 countries
Study dates
1 May 2024to 1 Jun 2028
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years
  • Written informed consent
  • Permanent, persistent, or paroxysmal spontaneous AF previously known or diagnosed during the index hospitalization.
  • Recent (≤3 months) symptomatic ischemic stroke.
  • Active and ongoing anticoagulation therapy at stroke onset assessed based on medical history (i.e. any therapeutic oral anticoagulation therapy [Vitamin K antagonist/DOAC according to prescription recommendations for AF; inadequate low-dose DOAC therapy allowed for inclusion] not stopped/paused for >48 hours due to any reason, i.e. medical intervention or non-adherence).
  • Active or planned long-term therapy with DOAC

Who cannot join

  • Contraindications to DOAC therapy
  • Life expectancy <1 year according to the opinion of the investigator
  • Stroke due to: Ipsilateral intra/extracranial high-grade stenosis, Isolated lacunar stroke, Other well-defined stroke aetiologies (i.e., endocarditis, vasculitis, Reversible Cerebral Vasoconstriction Syndrome [RCVS], Posterior Reversible Encephalopathy Syndrome [PRES], cerebral sinus venous thrombosis)
  • Previous persistent foramen ovale or atrial septum defect closure.
  • Rheumatic heart disease
  • Severe heart valve disease that requires treatment (severe aortic stenosis or regurgitation, severe mitral stenosis or regurgitation).
Show all 18Show fewer
  • Contraindications for TEE (relevant esophageal varices, esophageal stricture, history of esophageal cancer).
  • Cardiac or non-cardiac surgical procedure within 30 days of randomization
  • Enrolled in another investigation of a cardiovascular device or investigating secondary prevention therapy.
  • Severely reduced Left Ventricular Ejection Fraction (LVEF) <30%.
  • Severe renal impairment as described in the summary of medicinal product characteristics for the chosen DOAC (e.g. rivaroxaban, apixaban and edoxaban creatinine clearance <15 ml/min; dabigatran creatinine clearance <30 ml/min).
  • Hypertrophic cardiomyopathy
  • Intracardiac tumor
  • Ventricular thrombus
  • Acute cardiac decompensation
  • LAA is obliterated or surgically ligated
  • Persistent proximal LAA thrombus despite 4 weeks of anticoagulation (if a proximal thrombus in the LAA is found, anticoagulation with vitamin K antagonist (INR 2.5-3.5) may be started, and if the thrombus disappears, the patient may be eligible for LAAO)
  • Pregnancy or breastfeeding (pregnancy test in urine or blood to be performed at screening for women of childbearing potential)

Trial locations and contacts

34 sites in 6 countries. Contact the study team or a site near you to ask about taking part.

Lorenz Räber, Prof., MD, PhD contact

+41316320929

Lorenz.Raeber@insel.ch

David Seiffge, Prof., MD contact

+41316640509

david.seiffge@insel.ch

34 sites in 6 countries

Germany9 sites, 9 recruiting
  • Charité-Universitätsmedizin Berlin

    Berlin, 12203

    Christian H Nolte, Christian.nolte@charite.de

    Recruiting
  • Universitätsklinikum Bonn

    Bonn, 53127

    Gabor Petzold, Prof. Dr. med., gabor.petzold@ukbonn.de

    Recruiting
  • Universitätsmedizin Göttingen

    Göttingen, 37075

    Katrin Wasser, k.wasser@med.uni-goettingen.de

    Recruiting
  • Asklepios Klinik Altona

    Hamburg, 22763

    Joachim Röther

    Recruiting
  • University Hospital Heidelberg

    Heidelberg, 69120

    Christoph Gumbinger, Prof. Dr. med., Christoph.Gumbinger@med.uni-heidelberg.de

    Recruiting
  • Universitätsklinikum Leipzig

    Leipzig, 04103

    Prof. Dr. Dominik Michalski

    Recruiting
  • UKSH, Campus Lübeck

    Lübeck, Schleswig-Holstein, 26538

    Georg Royl, georg.royl@uni-luebeck.de

    Recruiting
  • Universitätsmedizin Mannheim

    Mannheim, 68167

    Prof. Dr. med. Angelika Alonso

    Recruiting
  • Universitätsklinikum Tübingen

    Tübingen, 72076

    Sven Poli, Prof. Dr. med., sven.poli@uni-tuebingen.de

    Recruiting

Other trials in Germany

Switzerland8 sites, 8 recruiting
  • University Hospital Basel

    Basel, 4031

    Mira Katan, Prof. Dr. med.

    Recruiting
  • Inselspital, University Hospital Bern

    Bern, 3010

    Lorenz Räber, Prof. Dr. med., PhD

    Recruiting
  • Hôpitaux universitaires de Genève

    Geneva, 1211

    Stéphane Noble, Prof. Dr. med.

    Not yet recruiting
  • Centre Hospitalier Universitaire Vaudois

    Lausanne, Vaude, 1011

    Davide Strambo, PD-MER Dr. med.

    Recruiting
  • Luzerner Kantonsspital

    Lucerne, 6000

    Manuel Bolognese, KD Dr. med.

    Not yet recruiting
  • Ente Ospedaliero Cantonale

    Lugano, Canton Ticino, 6900

    Marco Valgimigli, Prof. Dr. med., PhD

    Recruiting
  • Kantonsspital St. Gallen

    Sankt Gallen, 9007

    Gian Marco De Marchis, Prof. Dr. med.

    Recruiting
  • Stadtspital Zürich Triemli

    Zurich, 8063

    Marie-Luise Mono, PD Dr. med., marie-luise.mono@stadtspital.ch

    Recruiting

Other trials in Switzerland

Belgium6 sites, 6 recruiting
  • AZ Sint Jan Brugge

    Bruges, 8000

    Sofie De Blauwe, sofie.deblauwe@azsintjan.be

    Recruiting
  • Brussels University Hospital

    Brussels, 1090

    Lochy Stijn, stijn.lochy@uzbrussel.be

    Recruiting
  • UCLouvain - Cliniques universitaires Saint-Luc

    Brussels, 1200

    André Peeters, Andre.peeters@uclouvain.be

    Recruiting
  • HUmani CHU Charleroi-Chimay

    Charleroi, 6000

    Adel Aminian, adel.aminian@humani.be

    Recruiting
  • Universitair Ziekenhuis (UZ) Leuven

    Leuven, 3000

    Robin Lemmens, robin.lemmens@uzleuven.be

    Recruiting
  • CHU Liège Sart-Tilman

    Liège, 4000

    Géraldine Dasnoy-Sumell, MD, G.Dasnoy@chuliege.be

    Recruiting

Other trials in Belgium

Spain5 sites, 5 recruiting
  • Hosp. General Universario Dr. Balmis de Alicante

    Alicante, 03010

    Fernando Torres Mezcua, fernan.tormez@gmail.com

    Recruiting
  • Hosp. Barcelona Santa Creu y Sant Pau

    Barcelona, 08025

    Luis Prats Sanchez, LPratsS@santpau.cat

    Recruiting
  • Vall d'Hebron University Hospital

    Barcelona, 08035

    Jorge Pagola, jorge.pagola@vallhebron.cat

    Recruiting
  • Hosp. Clínic of Barcelona

    Barcelona, 08036

    Xavier Freixa, freixa@clinic.cat

    Recruiting
  • Hospital Clínico San Carlos (HCSC)

    Madrid, 28040

    Luis Nombela, luis.nombela@salud.madrid.org

    Recruiting

Other trials in Spain

United Kingdom5 sites, 5 recruiting
  • Addenbrooke's Hospital

    Cambridge

    Smitri Agarwal, MD, smriti.agarwal1@nhs.net

    Recruiting
  • Charing Cross Hospital

    London

    Lucio D'Anna, MD, MSc, PhD, ucio.d'anna@nhs.net

    Recruiting
  • St Bartholomew's Hospital

    London

    Mark James Early, MD, ChB, MB, mark.earley1@nhs.net

    Recruiting
  • St Thomas' Hospital

    London

    Ajay Bhalla, MD, Ajay.bhalla@gstt.nhs.uk

    Recruiting
  • University Hospitals Sessex NHS Trust

    Worthing

    David Hildick-Smith, MD, MRCP, FRCP, FSCAI, david.hildick-smith@nhs.net

    Recruiting

Other trials in United Kingdom

New Zealand1 site, 1 recruiting
  • Christchurch Hospital

    Christchurch, 8011

    Philip Adamson, Philip.adamson@cdhb.health.nz

    Recruiting

Other trials in New Zealand

About this study

Official title: Early Closure of Left Atrial Appendage for Patients With Atrial Fibrillation and Ischemic StrokE Despite Anticoagulation Therapy

Atrial fibrillation (AF) is one of the most common cardiac arrhythmias and cardioembolic stroke due to AF is its major complication. Direct oral anticoagulants (DOAC) reduce the risk of cardioembolism in patients with AF. Despite DOAC therapy, there is a significant residual stroke risk of 1-2%/year. Recent data from the Swiss Stroke Registry found 38% of patients with AF and ischemic stroke were on prior anticoagulant therapy (approximately 400 patients per year in Switzerland). The investigators found in a prior observational study, that patients with AF who have ischemic stroke despite anticoagulation are at increased risk of having another ischemic stroke (HR 1.6; 95% confidence interval, CI 1.1-2.1). Combining observational data from 11 international stroke centres, the investigators found that the majority of ischemic strokes despite anticoagulation in patients with AF is "breakthrough" cardioembolism (76% of patients) and only a minority of 24% is related to other causes unrelated to AF. Optimal secondary prevention strategy is unknown. The investigators have conducted two independent observational studies including together >4000 patients but did not identify any strategy (e.g. switch to different DOAC, additional antiplatelet therapy) that seems superior. A recent randomized controlled trial on surgical occlusion of the left atrial appendage (LAAO) found that LAAO may provide additional protection from ischaemic stroke in addition to oral anticoagulation. Triggered by this finding, the investigators performed a matched retrospective observational study and found that patients with AF and stroke despite anticoagulation who received a combined mechanical-pharmacological therapy (DOAC therapy + LAAO) had lower rates of adverse outcomes compared to those with DOAC therapy alone. Therefore, the investigators hypothesize that in patients with AF and ischemic stroke despite anticoagulant therapy, LAAO in addition to anticoagulation with a DOAC is superior to DOAC therapy alone. The investigators propose an international, multi-center randomized controlled two-arm trial to assess the effect of LAAO in patients with AF suffering from strokes despite anticoagulation therapy and without competing stroke etiology. The investigators will use the PROBE design with blinded endpoint assessment. The investigators will enrol patients with non-valvular AF and a recent ischemic stroke despite anticoagulation therapy at stroke onset. Patients will be randomized 1:1 to receive LAAO + DOAC therapy (experimental arm) or DOAC therapy alone (standard treatment arm). The primary endpoint is the first occurrence of a composite outcome of recurrent ischemic stroke, systemic embolism and cardiovascular death during follow-up. Secondary outcomes include individual components of the primary composite outcome, safety outcomes (i.e. symptomatic intracranial haemorrhage, major extracranial bleeding, serious device- or procedure-related complication), functional outcome (modified Rankin Scale) and patient-oriented outcomes. The minimum follow-up is 6 months and all patients will receive follow-ups every 6 months until end of study, the maximal follow-up will be 48 months. Based on prior observational data from the investigators' group and others (5 observational studies, >5000 patients), the investigators estimate the proportion of patients with the primary outcome in the standard treatment arm to be 18% in the first year and 9% in the second year (=cumulative 27% after 2 years). A relative risk reduction of 40% at 2 years would be clinically relevant. Based on these assumptions and a log-rank test, the investigators would need 98 events for a power of 80% at an alpha-level of 5%. Assuming a recruitment rate of 52, 118, 156 and 156 patients in years 1 to 4, an additional 6 months of follow-up (mean follow-up time of 2.1 years) and a uniform drop-out rate of 7.5% per year, 482 patients would need to be enrolled. How to treat patients with an ischemic stroke despite anticoagulation is a major yet unresolved clinical dilemma. This trial has the potential to answer the question whether LAAO plus DOAC therapy is superior to current standard of care for patients with AF who have ischemic stroke despite anticoagulation.

Being tested
Left atrial appendage Occlusion, DOAC
Keywords
Stroke, Direct oral anticoagulation, Left atrial appendage occlusion
Medical subject headings
Ischemic Stroke, Atrial Fibrillation, Stroke

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Left atrial appendage OcclusionProcedure or surgery

    Left atrial appendage Occlusion and therapy with direct oral anticoagulants. Choice of DOAC is at the discretion of the treating physician.

  • DOACDrug

    Therapy with direct oral anticoagulants. Choice of DOAC is at the discretion of the treating physician.

Study groups in NCT05976685
Study groupRoleWhat they receive
LAAO and DOAC therapyExperimentalLeft atrial appendage occlusion and therapy with direct oral anticoagulants
Receives: Procedure: Left atrial appendage Occlusion; Drug: DOAC
DOAC therapy onlyOtherTherapy with direct oral anticoagulants alone
Receives: Drug: DOAC

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Composite of recurrent ischemic stroke, systemic embolism, or cardiovascular death (whatever comes first).

    The primary endpoint is the first occurrence of a composite outcome of recurrent ischemic stroke, systemic embolism and cardiovascular death during follow-up. Stoke is defined as - New sudden focal neurological deficit of presumed cerebrovascular aetiology, occurring > 24 hours after the index ischaemic stroke, that persisted beyond 24 hours and was not due to another identifiable cause 18 (transient ischaemic attack (TIA), defined as a transient episode of neurologic dysfunction caused by focal brain, spinal cord, or retinal ischaemia without cerebral infarction on imaging, is not judged as stroke) and/or by brain imaging (CT or MRI). Systemic embolism is defined as abrupt vascular insufficiency associated with clinical or radiological evidence of arterial occlusion of an extremity or organ in absence of another likely mechanism (e.g. atherosclerosis, instrumentation or trauma). Cardiovascular death is defined as any death that is due to a vascular cause.

    Measured: 6 months

Secondary outcomes (12)
  1. Recurrent ischemic stroke

    Stoke is defined as - New sudden focal neurological deficit of presumed cerebrovascular aetiology, occurring > 24 hours after the index ischaemic stroke, that persisted beyond 24 hours and was not due to another identifiable cause 18 (transient ischaemic attack (TIA), defined as a transient episode of neurologic dysfunction caused by focal brain, spinal cord, or retinal ischaemia without cerebral infarction on imaging, is not judged as stroke) and/or by brain imaging (CT or MRI).

    Measured: 6 months

  2. Systemic embolism

    Systemic embolism is defined as abrupt vascular insufficiency associated with clinical or radiological evidence of arterial occlusion of an extremity or organ in absence of another likely mechanism (e.g. atherosclerosis, instrumentation or trauma).

    Measured: 6 months

  3. Cardiovascular death

    Cardiovascular death is defined as any death that is due to a vascular cause.

    Measured: 6 months

  4. Symptomatic intracranial hemorrhage

    A relevant symptomatic intracranial haemorrhage, this includes subdural, epidural, subarachnoidal and intracerebral haemorrhage, is defined as haemorrhage that leads to a clinical worsening and hospitalisation and is assessed by the treating physician to be likely the cause of the new neurological symptom or the death. Intracerebral haemorrhage due to a trauma will not be considered.

    Measured: 6 months

  5. Major extracranial bleeding (ISTH)

    Definition released by the International Society of Thrombosis and Haemostasis (ISTH): clinically overt bleeding which was fatal or associated with any of the following: (a) a fall in hemoglobin level of 2 g/dL or more or documented transfusion of at least 2 units of packed red blood cells, (b) involvement of a critical anatomical site (intracranial, spinal, ocular, pericardial, articular, intramuscular with compartment syndrome, retroperitoneal).

    Measured: 6 months

  6. Procedure-related death

    All-cause death within 30 days after randomization or during the index procedure hospitalization

    Measured: 6 months

  7. Serious device- or procedure-related complication

    7 days post-index procedure for device group subjects

    Measured: 6 months

  8. All-cause hospitalization

    Any hospital stay of at least 24 hours

    Measured: 6 months

  9. Cause-specific hospitalization

    Any hospital stay of at least 24 hours or which the primary admitting diagnosis was for heart failure, stroke, bleeding, atrial fibrillation, repeat AF-ablations, periprocedural complication, other cardiovascular causes

    Measured: 6 months

  10. Global health

    Measured by PROMIS (Patient-reported Outcomes Measurement Information System) Adult Global Health; continuous

    Measured: 6 months

  11. Global safety

    Measured by FeelSaveScale; continuous

    Measured: 6 months

  12. Functional neurological outcome

    Modified Rankin Scale; ordinal

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Aug 2023
  2. Study start1 May 2024
  3. Primary completion1 Jan 2028 (estimated)
  4. Study completion1 Jun 2028 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
482 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05976685
Sponsor's protocol ID
2023-02340
Other IDs
2023
Acronym
ELAPSE
Status last verified
Apr 2026
First submitted
27 Jul 2023
Last updated
6 Nov 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Left atrial appendage Occlusion and DOAC in people with Ischemic Stroke and Atrial Fibrillation, run by Insel Gruppe AG, University Hospital Bern at 34 sites in 6 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 18 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 6 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 34 sites in Germany, Switzerland, Belgium, Spain, United Kingdom and 1 more country. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Lorenz Räber, Prof., MD, PhD (+41316320929, Lorenz.Raeber@insel.ch), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Composite of recurrent ischemic stroke, systemic embolism, or cardiovascular death (whatever comes first). (time frame: 6 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Nov 2026.

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