Cardiac resynchronization therapy (CRT) is a recommended treatment for selected patients with symptomatic heart failure (HF). Although most treated patients show a benefit from CRT, a lack of response is observed for about 25-30% of them whatever the response criteria used either based on the clinical status (NYHA class, Packer clinical composite score) or on ventricular remodeling parameters assessed by echography (Left ventricle end of systole volume). This rate has remained remarkably stable since the therapy started and has motivated many studies to better understand the underlying physiopathology and the CRT action mechanisms. Among the various research axes to improve CRT response and responders rate, increasing the number of pacing sites in an attempt to better homogenize the cardiac mechanical activity has been evaluated. A configuration with two RV leads and one LV lead was tested acutely in three studies. In all cases, it demonstrated a significant improvement of cardiac performance whether assessed by echographic parameters or LV dp/dt measurements. Additionally feasibility of this approach for long term CRT delivery was demonstrated during a previous study. First results with triple-site ventricular stimulation are encouraging and its clinical efficacy should now be tested on a larger population in order to conclude on its interest for CRT candidates.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
Cardiac resynchronization therapy implantation will be done for patient with symptomatic heart failure
Cardiac resynchronization therapy with stimulation of 3 ventricular sites
Cardiac resynchronization therapy with stimulation of 2 ventricular sites
Standard Echocardiography will de bone for patient
Rouen University Hospital
Rouen, France
Difference from baseline in Left Ventricular End-Systolic Volume
Left Ventricular End-Systolic Volume will be evaluated using echocardiography
Time frame: 12 months
Difference from baseline in left ventricular remodelling
Left ventricular remodelling will be evaluated using echocardiography
Time frame: 12 months
Number of patients alive
Time frame: 12 months
Number of adverse events
Time frame: 12 months
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