The present trial is undertaken as a pilot study on selected patients, to evaluate the ability of acute hemodynamic testing to optimize pacing therapy and to predict the response of Obstructive Hypertrophic Cardiomyopathy (OHCM) to pacing, in terms of reduction of Left Ventricular Outflow Tract (LVOT) pressure gradient and functional capacity improvement. The Primary Objective is to demonstrate a long-term reduction in LVOT obstruction at rest and/or after Valsalva/Exercise \> 30% in patients responding to acute stimulation test
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
To evaluate the ability of acute hemodynamic testing to optimize pacing therapy and to predict the response of HOCM to pacing
Istituto Auxologico Italiano
Milan, Italy
RECRUITINGReduction of LVOT pressure gradient
Long-term reduction in LVOT obstruction at rest and/or after Valsalva/Exercise \> 30% in patients responding to acute stimulation test
Time frame: 3 months
Clinical improvement: change in NYHA class
Improvement of NYHA class
Time frame: 6-12 months
Clinical improvement: change in exercise capacity
6-minutes walking test
Time frame: 6-12 months
Clinical improvement: change in peak VO2
Improvement in peak VO2
Time frame: 6-12 months
Clinical improvement: change in NT-proBNP concentration
Reduction in NT-proBNP concentration
Time frame: 6-12 months
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