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Study identifier: NCT05353140 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

LAAO Versus NOAC in Patients with AF and PCI

Condition: Atrial Fibrillation · Percutaneous Coronary Intervention  ·  Sponsor: Xijing Hospital

PhaseNA
Planned participants1386
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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,…

This description comes directly from the study's public registry record.

Talk to the study team

Chao Gao, M.D., Ph.D.  ·  +86-18629551066  ·  woshigaochao@gmail.com

Ruining Zhang, BSc  ·  +86-15802990370  ·  ruining-zhang@qq.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ling TaoXi'an, Shannxi, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05353140