Heart Failure Clinical Trial
Official title:
Randomized, Crossover Study of the Effects of MultiPoint Left Ventricular Pacing on Neurohormonal Activation.
This study will examine the additional clinical benefit conferred by multipoint pacing (MPP) compared to standard CRT over a period of 3 months. Patients will be randomized to MPP ON vs. OFF and followed for a total of 6 months. This includes two crossover periods for each pacing modality (MPP on vs. off).
Cardiac resynchronization therapy (CRT) is limited by a high proportion of non-responders.
Pacing activation from multiple separated left ventricular (LV) sites might improve the
depolarization pattern, thereby promoting more physiological activation. To explore the
effect of MPP on cardiac neuro-hormonal activity, the investigators will enroll approximately
30 patients who already underwent CRT-D implantation with a quadripolar LV lead connected to
a device capable of MPP.
This pilot study will have a randomized, double-blind, cross-over design. Patients will be
randomized to receive either standard biventricular pacing (MPP-OFF) or MPP (MPP-ON) within
4-6 months following the implantation procedure. Each subject will crossover to the other
study group after three months. The baseline evaluation should be acquired prior to the
device being programmed to the randomized setting. Repeat evaluations will be performed at
the end of each 3 month crossover period.
Participation in this study will last approximately 6 months. Patients, as well as
investigators other than the EP physicians, will be blinded to the pacing mode.
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