Stroke Clinical Trial
Official title:
Amplatzer™Amulet™ Observational Post-Market Study
This was a prospective, multicenter, observational, nonrandomized study to compile real world outcome data on the use of the Amulet™ device in non-valvular atrial fibrillation (NVAF) subjects. The study was designed to follow the Instructions For Use (IFU) to gather data on the implant procedure through two years of follow up with the Amulet™ device in a commercial clinical setting."
A total of 1088 subjects were enrolled in the study at 61 sites internationally, outside the
United States.
The study assessed acute and late serious adverse events and reports the rate of stroke and
bleeding events through 2 years. No formal hypothesis were tested for this observational
post-market study.
Each patient was followed at study visits at baseline, implant, 1-3 months, 6 months, 12
months, and 24 months post implant."
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