A Real-World Study to Observe Outcomes of Patients Undergoing Closure with the Amplatzer Amulet Left Atrial Appendage Occluder

Brief description of study

The primary objective of this clinical study is to characterize real-world procedural and safety outcomes on the Amulet device in the United States in the hands of routine implanters. To align with previous Amulet investigations and current LAAO standard of care (SOC), acute procedural safety and long-term outcomes will be collected through 24 months of follow-up.

Clinical Study Identifier: s23-00852
Principal Investigator: Larry A Chinitz.

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