7
Participants
Start Date
January 31, 2006
Primary Completion Date
January 31, 2008
Study Completion Date
January 31, 2016
CRT device implant
The purpose of this study is to collect information on patients with chronic heart failure who have already been identified by their physician as candidates for CRT. All tests, including device implantation are standard of care for patients undergoing CRT. The only test involved in this study that is not standard of care is the quality of life questionnaire. Patients who undergo CRT system implant will be followed post-implant (up to 1 week), and at one month, three months, six months and twelve months. The only test involved in this study that is not standard of care is the quality of life questionnaire.
University of Utah, Salt Lake City
University of Utah
OTHER