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Clinical Trial Summary

The purpose of this study is to gather evidence about the safety and feasibility of performing the implant procedure for the Reveal Insertable Cardiac Monitor (ICM) in an office or clinic setting rather than the traditional hospital operating room, cardiac catheterization or electrophysiology (EP) laboratory setting.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01168427
Study type Observational
Source Medtronic Cardiac Rhythm and Heart Failure
Contact
Status Completed
Phase N/A
Start date August 2010
Completion date May 2011

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