Key result
The AdaptResponse trial is designed to randomize approximately 3,000 patients to evaluate whether the AdaptivCRT algorithm reduces all-cause mortality and HF decompensation versus conventional CRT.
Why the study?
Does a CRT system with the AdaptivCRT algorithm reduce the composite of all-cause mortality and intervention for HF decompensation compared to conventional CRT in patients with a CRT indication, LBBB, and normal AV conduction?
Population
Approximately 3,000 patients with a cardiac resynchronization therapy indication, left bundle branch block…
Comparison
CRT system containing the AdaptivCRT algorithm vs Conventional CRT
Design
RCT, 1:1 fashion, single-blinded
Follow-up
event-driven
Authors
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Supports adaptive CRT in LBBB patients with normal AV conduction; extends randomized evidence for optimized resynchronization.
RCT (n=3,000)
Single-blind
1:1
Yes
Does a CRT system with the AdaptivCRT algorithm reduce the composite of all-cause mortality and intervention for HF decompensation compared to conventional CRT in patients with a CRT indication, LBBB, and normal AV conduction?
The AdaptResponse trial is designed to determine if the AdaptivCRT algorithm improves clinical outcomes compared to conventional CRT in patients with LBBB and normal AV conduction.
Filippatos et al. (2017) conducted an RCT in Heart failure (n=3,000). AdaptivCRT algorithm vs. Conventional CRT was evaluated on Composite of all-cause mortality and intervention for HF decompensation. The AdaptResponse trial is designed to randomize approximately 3,000 patients to evaluate whether the AdaptivCRT algorithm reduces all-cause mortality and HF decompensation versus conventional CRT.
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