Summary of Purpose
This will be a prospective, multicenter, observational, non-randomized study to compile real world outcome data on the use of the Amulet™device in non-valvular atrial fibrillation (NVAF) subjects. The study is 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.Read More →
The following dates are available for this trial. Trial information last updated on 19 September 2016.
|1 Apr 2015||27 Apr 2015||1 Nov 2016||1 Dec 2018||1 Jul 2016||Unavailable|
|Start Date||First Received||1st Completion||Completion||Verification||Results|
- St. Jude Medical Lead
- Perspective: Prospective
- Sampling: Non-Probability Sample