Principal
Investigator:
Peter Fattal, MD
(MCVI)
Sub-Investigators:
Asim Yunus, MD
Sponsor:
Medtronic
Study Purpose:
PRECEDE-HF: Prospective, Randomized Evaluation of
Cardiac CompassŪ with OptiVolŪ in the Early Detection of Decompensation Events
for Heart Failure
Objective:
To collect data to compare subjects whose heart failure is managed using Cardiac
Compass with OptiVol combined with standard treatment methods (called the Access
Group) to subjects whose heart failure is managed by standard treatment methods
only (called the Control Group). This comparison will evaluate whether the
additional monitoring provided by Cardiac Compass keeps subjects out of the
hospital longer or delays the time to death.
Status:
Active enrollment
If you have any
questions, please feel free to contact the coordinators, and they will be happy
to answer any questions you have regarding this study.
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