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Clinical Trials/NCT03108872
NCT03108872
Unknown
Not Applicable

Long Term Clinical Outcomes of Left Atrial Appendage Occlusion Versus New Oral Anticoagulants for Stroke Prevention in Patients With Non-valvular Atrial Fibrillation; From Korean Multicenter Registry

Sejong General Hospital1 site in 1 country300 target enrollmentMay 23, 2017

Overview

Phase
Not Applicable
Intervention
left atrial appendage occlusion
Conditions
Atrial Fibrillation
Sponsor
Sejong General Hospital
Enrollment
300
Locations
1
Primary Endpoint
Primary effectiveness endpoint
Last Updated
8 years ago

Overview

Brief Summary

We will compare long-term effectiveness and safety in patients with atrial fibrillation treated with left atrial appendage occlusion versus new oral anticoagulants to prevent ischemic stroke from multicenter registry data

Detailed Description

Atrial fibrillation (AF) is associated with a substantial risk of stroke and systemic embolism. Vitamin K antagonists are highly effective in preventing stroke in patients with atrial fibrillation and high risk of ischemic stroke. However, their use is limited by a narrow therapeutic range, increased risk of intracranial hemorrhage, the need for continuous monitoring of INR, and drug or food interaction. New oral anticoagulants (NOACs), the direct thrombin inhibitor and the factor Xa inhibitor, have settled these limitations of warfarin therapy. In four pivotal phase 3 clinical trials and their meta-analysis, NOACs have been shown to significantly reduce ischemic stroke, intracranial hemorrhage, and mortality, and had similar major bleeding as for warfarin in patients with non-valvular atrial fibrillation (NVAF). Another new treatment strategy for prevention of stroke is left atrial appendage occlusion (LAAO). Left atrial appendage has been considered to be an origin of thrombi more than 90% of cases. The concept that exclusion of LAA from the circulation reduces the risk of stroke in patients with NVAF is therefore being tested in clinical studies. LAAO with Watchman device and only aspirin were proved to be non-inferior to warfarin for ischemic stroke prevention or systemic embolism. And, LAAO reduced significantly cardiac death and hemorrhagic stroke compared to warfarin in a long-term follow up. Up to date, there was no study to compare long-term clinical outcomes between LAAO and NOACs, which are two new treatment strategies for stroke prevention in patients with NVAF.

Registry
clinicaltrials.gov
Start Date
May 23, 2017
End Date
October 30, 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Sejong General Hospital
Responsible Party
Principal Investigator
Principal Investigator

Hyun Jong Lee

Principle Investigator

Sejong General Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with atrial fibrillation, who LAAO or NOAC to prevent ischemic stroke or systemic embolism
  • Patients with CHA2DS2-VASc score \>1

Exclusion Criteria

  • Patients who failed to successfully implant LAAO
  • Patients who receive new oral anticoagulant less than 6 months without clinical events
  • Patients with mitral stenosis more than mild grade
  • Patients with prosthetic heart valve

Arms & Interventions

LAAO group

One-hundred consecutive patients who underwent left atrial appendage occlusion from October 2010 to March 2015 in 5 Korean tertiary cardiovascular centers will be retrospectively registered.

Intervention: left atrial appendage occlusion

NOAC group

Two-hundred age-, sex-, CHA2DS2-VASc score- and HAS-BLED score- matched control will be selected with a 1:2 ratio among all patients treated with new oral anticoagulants to prevent ischemic events from 5 centers during same periods

Intervention: New oral anticoagulants

Outcomes

Primary Outcomes

Primary effectiveness endpoint

Time Frame: During 4 years

The composite of cardiovascular or unexplained death, or ischemic stroke, or systemic embolism

Primary safety endpoint

Time Frame: During 4 years

Major bleeding or Serious device-related complications

Secondary Outcomes

  • Cardiovascular or unexplained death(During 4 years)
  • Serious device-related complications(During 4 years)
  • Major bleeding(During 4 years)
  • Ischemic stroke or systemic embolism(During 4 years)
  • Hemorrhagic stroke(During 4 years)

Study Sites (1)

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