Medtronic Shock-Less Study
Status: | Archived |
---|---|
Conditions: | Peripheral Vascular Disease |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | Any |
Updated: | 7/1/2011 |
Start Date: | April 2009 |
End Date: | October 2013 |
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.
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.
We found this trial at
35
sites
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1351 Kimberly Rd
Bettendorf, Iowa 52722
Bettendorf, Iowa 52722
(563) 355-7733
Hematology Oncology Associates of the Quad Cities
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