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Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programming

Cardiovascular Disease Clinical Trial

Official title:
Medtronic Shock-Less Study on Physician Utilization of Shock Reduction Programming

Clinical Trial Summary

The purpose of this clinical trial is to determine whether periodic therapy programming reports illustrating physician usage of shock reduction programming can increase utilization of recommended programming guidelines for defibrillators.

Clinical Trial Description

Shocks delivered to patients by defibrillators, while life-saving, can create anxiety, pain and decrease quality of life. Previous studies have shown that device programming and features can safely reduce the number of shocks patients receive. This study will explore the extent to which physicians use these programming and features. It will determine whether repeat and frequent awareness to how they program their own subjects and the programming trends of all enrolled subjects will change their programming patterns. This will be accomplished by understanding physicians' device programming behaviors and providing reports as a tool to help physicians manage their subjects and provide shock reduction programming recommended by previous publications. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00856349
Study type Observational
Source Medtronic Cardiac Rhythm Disease Management
Contact
Status Completed
Phase N/A
Start date April 2009
Completion date March 2013
View Details
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