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Study identifier: NCT05960721 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Low-dose NOAC Versus GDMT After LAAO

Condition: Atrial Fibrillation  ·  Sponsor: Xijing Hospital

PhaseNA
Planned participants4220
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The increased risk of Atrial fibrillation (AF) regarding thromboembolic stroke is predominantly due to the formation and embolization of clots from within the left atrial appendage (LAA). Percutaneous left atrial appendage occlusion (LAAO) is a nonpharmacological strategy for stroke prevention in patients with AF. Data from randomized trials, including PROTECT-AF, PREVAIL, and Prague-17, have suggested that LAAO has comparable efficacy to warfarin or NOACs. Considering these results, LAAO was recommended by the American College of Cardiology (ACC) and European Society of Cardiology (ESC) guidelines as a non-pharmacological stroke prevention strategy for patients with NVAF who have contraindications or are unsuitable for OAC. The PROTECT-AF and PREVAIL trials stipulated the use of standardized antithrombotic medications which were designed to minimize the risk of stroke, systemic embolism, or device-related thrombosis. This antithrombotic strategy was subsequently endorsed by the guidelines, briefly, patients with LAAO were discharged on warfarin and aspirin for 45 days post-LAAO, if there was no leak or a leak ≤5 mm under transesophageal echocardiography (TEE) at 45-day follow-up, antithrombotic strategies shall switch to dual antiplatelet therapy (DAPT) until 6 months post-LAAO, and then aspirin thereafter. Although LAAO was recommended by medical societies, previous patient-level meta-analyses have implied that compared with oral anticoagulation, LAAO had significantly mo…

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/NCT05960721