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.
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
- Type of treatment
- Pill or oral medicine, Surgery or procedure
- 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.
34 sites in 6 countries
Germany9 sites, 9 recruiting
- 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
Switzerland8 sites, 8 recruiting
- Recruiting
University Hospital Basel
Basel, 4031
Mira Katan, Prof. Dr. med.
- Recruiting
Inselspital, University Hospital Bern
Bern, 3010
Lorenz Räber, Prof. Dr. med., PhD
- Not yet recruiting
Hôpitaux universitaires de Genève
Geneva, 1211
Stéphane Noble, Prof. Dr. med.
- Recruiting
Centre Hospitalier Universitaire Vaudois
Lausanne, Vaude, 1011
Davide Strambo, PD-MER Dr. med.
- Not yet recruiting
Luzerner Kantonsspital
Lucerne, 6000
Manuel Bolognese, KD Dr. med.
- 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
Belgium6 sites, 6 recruiting
- 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
Spain5 sites, 5 recruiting
- 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
United Kingdom5 sites, 5 recruiting
- 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
New Zealand1 site, 1 recruiting
- Recruiting
Christchurch Hospital
Christchurch, 8011
Philip Adamson, Philip.adamson@cdhb.health.nz
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.
- Conditions
- Ischemic Stroke, Atrial Fibrillation
- 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 group | Role | What they receive |
|---|---|---|
| LAAO and DOAC therapy | Experimental | Left atrial appendage occlusion and therapy with direct oral anticoagulants Receives: Procedure: Left atrial appendage Occlusion; Drug: DOAC |
| DOAC therapy only | Other | Therapy 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.
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)
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
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
Cardiovascular death
Cardiovascular death is defined as any death that is due to a vascular cause.
Measured: 6 months
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
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
Procedure-related death
All-cause death within 30 days after randomization or during the index procedure hospitalization
Measured: 6 months
Serious device- or procedure-related complication
7 days post-index procedure for device group subjects
Measured: 6 months
All-cause hospitalization
Any hospital stay of at least 24 hours
Measured: 6 months
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
Global health
Measured by PROMIS (Patient-reported Outcomes Measurement Information System) Adult Global Health; continuous
Measured: 6 months
Global safety
Measured by FeelSaveScale; continuous
Measured: 6 months
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.
- First posted4 Aug 2023
- Study start1 May 2024
- Primary completion1 Jan 2028 (estimated)
- Study completion1 Jun 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Ischemic StrokeStudies of the same condition, open and under way.
- More trials run by Insel Gruppe AG, University Hospital BernThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Insel Gruppe AG, University Hospital Bern
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Lorenz Räber, Prof., MD, Principal investigator, Cardiovascular Center, Inselspital Bern
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
Study at a glance
From the registry record, last updated by the sponsor on 6 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Closure of Left Atrial Appendage for Patients With Atrial Fibrillation and Ischemic StrokE Despite Anticoagulation Therapy
- ClinicalTrials.gov ID
- NCT05976685
- Acronym / sponsor ID
- ELAPSE / 2023-02340
- Conditions
- Ischemic Stroke, Atrial Fibrillation
- Keywords
- Stroke, Direct oral anticoagulation, Left atrial appendage occlusion
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 482 participants (estimated)
- Lead sponsor
- Insel Gruppe AG, University Hospital BernUniversity, hospital or other
- Study start
- 1 May 2024 (actual)
- Primary completion
- 1 Jan 2028 (estimated)
- Study completion
- 1 Jun 2028 (estimated)
- First posted
- 4 Aug 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| LAAO and DOAC therapy | Experimental | Procedure: Left atrial appendage Occlusion, Drug: DOACLeft atrial appendage occlusion and therapy with direct oral anticoagulants |
| DOAC therapy only | Other | Drug: DOACTherapy with direct oral anticoagulants alone |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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).
Key exclusion criteria (18 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Left atrial appendage OcclusionLeft atrial appendage Occlusion and therapy with direct oral anticoagulants. Choice of DOAC is at the discretion of the treating physician. | Procedure or surgery | LAAO and DOAC therapy |
| DOACTherapy with direct oral anticoagulants. Choice of DOAC is at the discretion of the treating physician. | Drug | DOAC therapy only, LAAO and DOAC therapy |
Primary outcome
Composite of recurrent ischemic stroke, systemic embolism, or cardiovascular death (whatever comes first).
Time frame: 6 months
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.
12 secondary outcomes
Recurrent ischemic stroke
Time frame: 6 months
Systemic embolism
Time frame: 6 months
Cardiovascular death
Time frame: 6 months
Symptomatic intracranial hemorrhage
Time frame: 6 months
Major extracranial bleeding (ISTH)
Time frame: 6 months
Procedure-related death
Time frame: 6 months
Serious device- or procedure-related complication
Time frame: 6 months
All-cause hospitalization
Time frame: 6 months
Cause-specific hospitalization
Time frame: 6 months
Global health
Time frame: 6 months
Global safety
Time frame: 6 months
Functional neurological outcome
Time frame: 6 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 Nov 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Lorenz Räber, Prof., MD principal investigator
Cardiovascular Center, Inselspital Bern
34 sites in 6 countries: see every site and its status.
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.