The primary objective of this study is to demonstrate that in patients with recuperated/normalized left ventricular function, defined as an ejection fraction (EF) ≥ 50%, after implantation of cardiac resynchronization therapy, device treatment is sufficient and neurohumoral blocker therapy can safely be withdrawn
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
RAAS blockers (combination of ACE-I/ARB and a mineralocorticoid receptor antagonist)
Ziekenhuis Oost Limburg
Genk, Limburg, Belgium
a > 15% increase in left ventricular end systolic volume
Time frame: at 12 months
- Incidence of HF related hospitalizations defined as admission to hospital / presentation to emergency room with need for parental therapy
Time frame: at 12 months
All cause mortality
Time frame: at 12 months
VO2 max change
Time frame: at 12 months
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