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LAAO Versus NOAC in Patients with AF and PCI

Left Atrial Appendage Occlusion Versus Novel Oral Anti-coagulation in Patients with Atrial Fibrillation and Percutaneous Coronary Intervention: a Randomized, Multicentre, Open-label, Non-inferiority Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05353140
Enrollment
1386
Registered
2022-04-29
Start date
2022-09-01
Completion date
2029-09-20
Last updated
2025-03-07

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

Conditions

Atrial Fibrillation, Percutaneous Coronary Intervention

Keywords

Left atrial appendage occlusion, Percutaneous coronary intervention, Novel oral anti-coagulation, Atrial Fibrillation

Brief summary

Atrial fibrillation (AF) coincides with coronary artery disease (CAD) shared common risk factors and pathophysiologic pathways. CAD affects approximately 25% of AF patient according to the trial Atrial Fibrillation Follow-up Investigation of Rhythm Management (AFFIRM), while in the Global Registry of Acute Coronary Events (GRACE) atrial fibrillation affected about 9% of patients with CAD. It is reported that approximately 5-8% of the patients who underwent PCI had concomitated atrial fibrillation. For AF patients who underwent PCI, both antiplatelet and antithrombotic medications are required for preventing stent thrombosis and ischemic stroke, leading to an increased risk of bleeding. Finding a safe and effective balance between the risk of ischaemic events and bleeding complications is challenged by the shared risk factors for either event such as advanced age, congestive heart failure, hypertension, diabetes, previous stroke, etc.. Previous pivotal trials have shown that in patients with atrial fibrillation and requiring antiplatelet treatment, a NOAC plus clopidogrel regimen was associated with a lower incidence of bleeding events as compared with a warfarin-based triple antithrombotic strategy. Therefore, the current expert opinions and consensus of North American Societies recommend a NOAC plus a P2Y12 inhibitor in patients with AF and PCI. However, the NOAC plus clopidogrel strategy still led to 16.8% of clinically significant bleeding (PIONEER AF-PCI). Consequently, the compliance of OAC/NOAC is commonly suboptimal among PCI patients who require an antithrombotic strategy for AF. Percutaneous left atrial appendage occlusion (LAAO) is a non-pharmacological strategy for stroke prevention in patients with AF. Both randomized data and registries have confirmed it can be an alternative to oral anticoagulation in patients with nonvalvular AF. Current guidelines recommend LAAO for patients with NVAF who have contraindications or are unsuitable for long-term OAC. Considering the unique high risk of AF patients with PCI, LAAO may be an attractive treatment option by obviating the need for combined oral anticoagulation and antiplatelet therapy. However, so far there is no data from neither randomized cohorts nor real-world registries showing if LAAO can be a safe and effective alternative strategy compared to VKA/NOAC for stroke prevention in AF patients who underwent PCI. The PROTECT AF and PREVAIL studies showed that the percutaneous LAAO was non-inferior to warfarin therapy, and the PRAGUE-17 trial showed non-inferior to direct oral anticoagulants, however, the small sample size of these trials limited further subgroup analyses of the PCI sub-population. In the NCDR registry, which is the largest cohort of LAAO up to now, 20.3% of the LAAO patients had a prior myocardial infarction. However, the proportion of stent implantation was not reported. Among previous trials, the proportion of patients with coronary artery disease ranged from 28.5% to 47.5%. The large number of AF patients with CAD warrant the optimal stroke prevention strategy to be assessed in this population. The primary goal of the proposed study is to investigate if the non-inferiority would be met for the LAAO when compared to NOACs in NVAF patients with PCI in terms of a composite endpoint of any death, any stroke, any myocardial infarction, systemic embolism at 12 months. In addition, the powered key secondary will also have 80% of power to show superiority for the LAAO when compared to NOACs in terms of BARC type 2, 3, or 5 bleeding events at 36 months.

Interventions

DEVICEThe WATCHMAN/WATCHMAN FLX device

Watchman device was an umbrella-shaped, self-expanding, nitinol structure with a porous partial polyethylene terephthalate membrane (160 um mesh) and 10 struts. The membrane portion of the structure faces into the body of the left atrial to block embolization of thrombus and provide scaffolding on which endothelialization can occur. The On July 21st, 2020, the FDA approved the next generation LAAO device, named Watchman FLX. This newiteration of the Watchman LAAO platform offers full capability of recapture and redeployment of the device, decreasedmetallic exposure, an increased number of contact points for sealing, a fully rounded delivery shape, and precision anchors designed to provide optimal device engagement with the LAA.

DRUGRivaroxaban + Clopidogre

Previous pivotal trials have shown that in patients with atrial fibrillation and requiring antiplatelet treatment, a NOAC plus clopidogrel regimen was associated with a lower incidence of bleeding events as compared with a warfarin-based triple antithrombotic strategy. Therefore, the current expert opinions and consensus of North American Societies recommend a NOAC plus a P2Y12 inhibitor in patients with AF and PCI. In the present study, Rivaroxaban + Clopidogre are required for 45 days in LAAO group after LAAO.

Aspirin + Clopidogrel are required from 46 days to 12 months after LAAO.

Sponsors

Xijing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

1. Successful PCI for unstable angina or CCS 2. Non-valvular atrial fibrillation 3. Concomitant at least one of the following conditions: congestive heart failure, hypertension, ≥65yrs, diabetes, previous stroke, TIA or thromboembolism 4. Eligible for long-term novel oral anti-coagulation (NOAC) therapy 5. Able to understand and provide informed consent and comply with all study procedures/medications

Exclusion criteria

Patients who meet any of the following criteria will be disqualified from participation in the study: Clinical

Design outcomes

Primary

MeasureTime frameDescription
Major adverse cardiac and cerebrovascular events (MACCE)12 monthsMACCE define as a composite endpoint of any death, any stroke, any myocardial infarction (MI), and systemic embolism (SE).

Secondary

MeasureTime frameDescription
BARC type 2, 3 or 5 bleeding events36 monthsPowered Key secondary endpoint, Bleeding Academic Research Consortium (BARC) defined type 2, 3, 5 bleeding events

Other

MeasureTime frameDescription
BARC type 2 bleeding events45days, 3, 6, 12, 24, 36, 60monthsBleeding Academic Research Consortium (BARC) defined type 2 bleeding events
Procedure related major complications30 days post LAAODefined according to the the Munich consensus document on definitions, endpoints, and data collection requirements for LAAO clinical studies
A composite endpoint of any death, any stroke, and systemic embolism45days, 3, 6, 12, 24, 36, 60monthsA composite endpoint of any death, any stroke, and systemic embolism
Any death45days, 3, 6, 12, 24, 36, 60monthsAny death
Any stroke45days, 3, 6, 12, 24, 36, 60monthsAny stroke
Any myocardial infarction (MI)45days, 3, 6, 12, 24, 36, 60monthsAny myocardial infarction (MI)
Device/Technical/Procedural successful rate30 days post LAAODevice success was defined as the device deployed and implanted in the correct position. Technical success was defined as the exclusion of the left atrial appendage, with no device-related complications and no leak \>5 mm. Procedural success was defined as technical success and no procedure-related complications
Systemic embolism (SE)45days, 3, 6, 12, 24, 36, 60monthsSystemic embolism (SE)
BARC type 2, 3 or 5 bleeding events45days, 3, 6, 12, 24, 60monthsBleeding Academic Research Consortium (BARC) defined type 2, 3, 5 bleeding events
Patient oriented Composite Endpoint (PoCE)45days, 3, 6, 12, 24, 36, 60monthsPatient oriented Composite Endpoint (PoCE), defined as the composite of any death, any myocardial infarction, any stroke, any revascularization, and systemic embolism, and its individual components
Net adverse clinical events (NACE)45days, 3, 6, 12, 24, 36, 60monthsNet adverse clinical events (NACE), defined as the composite of any death, any myocardial infarction, any stroke, any revascularization, systemic embolism, and BARC type 3 or 5 bleeding events and its individual components
Acute/subacute/early thrombosis45days, 3, 6, 12, 24, 36, 60monthsAcute, subacute, or early thrombosis
TIMI major bleeding and/or minor bleeding45days, 3, 6, 12, 24, 36, 60monthsThrombolysis in Myocardial Infarction (TIMI) defined major bleeding and/or minor bleeding
ISTH major bleeding and/or clinically relevant minor bleeding45days, 3, 6, 12, 24, 36, 60monthsInternational Society on Thrombosis and Haemostasis (ISTH) defined major bleeding and/or clinically relevant minor bleeding
Patient adherence to allocated medication45days, 3, 6, 12, 24, 36, 60monthsPatient adherence to allocated medication, defined as the use of medication strategies of this trial on 80% of the time in therapeutic range
Neurological assessment45days, 3, 6, 12, 24, 36, 60monthsNeurological assess by modified Rankin Scale (mRS) score: The mRS is used to assess long-term function following a stroke event. Complete a mRS Stroke Assessment Worksheet at approximately 90 days following the stroke for a long-term functional assessment. Scores: 0, No symptoms; 1, No significant disability. Able to carry out all usual activities, despite some symptoms; 2, Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities; 3, Moderate disability. Requires some help, but able to walk unassisted; 4, Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted; 5, Severe disability. Requires constant nursing care and attention, bedridden, incontinent; 6, Dead.
Quality of life assessments45days, 3, 6, 12, 24, 36, 60monthsQuality of life assess by Five-level EuroQol five-dimensional questionnaire (EQ-5D-5L): EQ-5D-5L is a simple and general health measurement method. In the description part, the health status will be described in 5 dimensions. The questionnaire require subjects to choose the most suitable option for themselves from each dimension according to their health status. The visual analog scale section is on a vertical scale, recording subjects' self-assessed health status.
Target lesion failure (TLF)45days, 3, 6, 12, 24, 36, 60monthsTarget lesion failure (TLF), defined as the composite of cardiac death, target vessel myocardial infarction (TV-MI), and clinically indicated target lesion revascularization (TLR), and its individual components
BARC type 3 or 5 bleeding events45days, 3, 6, 12, 24, 36, 60monthsBleeding Academic Research Consortium (BARC) defined type 3, 5 bleeding events

Countries

China

Contacts

Primary ContactChao Gao, M.D., Ph.D.
woshigaochao@gmail.com+86-18629551066
Backup ContactRuining Zhang, BSc
ruining-zhang@qq.com+86-15802990370

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026