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Clinical Trial Summary

The purpose of this study is to evaluate the safety and effectiveness of the Laminar Left Atrial Appendage Closure System to treat patients with non-valvular atrial fibrillation that cannot take, or a have a reason to seek an alternative, to anticoagulant medications.


Clinical Trial Description

Left atrial appendage closure (LAAC) is an approved therapy for stroke prevention in atrial fibrillation patients who are recommended for chronic oral anticoagulation therapy (OAC), but are non-eligible or have an appropriate rationale to seek a non-pharmacologic alternative to chronic oral anticoagulants in accordance with evidence-based decision-making criteria and current scientific guidelines. The objective of this study is to evaluate the safety and effectiveness of the Laminar Left Atrial Appendage Closure System to treat patients with non-valvular atrial fibrillation who are deemed appropriate for LAAC to reduce the risk of stroke and systemic embolism. Patients will be followed for 12 months after the procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05224375
Study type Interventional
Source Laminar, Inc.
Contact Bryan Petrisko, MS
Phone (707) 523-1950
Email bpetrisko@laminarlaa.com
Status Recruiting
Phase N/A
Start date December 9, 2021
Completion date May 2025

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