AdaptResponse Clinical Investigation Plan

AdaptResponse Clinical Investigation Plan
Recruiting
18 years - 99 years
All
Phase 4
1 Location

Brief description of study

The purpose of the research study is looking at a new algorithm (step by step approach) for patients with heart failure who are indicated for an BiV (biventricular) pacing device.

Detailed description of study

The purpose of this study is to test if patients with a new pacing algorithm, Adaptive Cardiac Resynchronization Therapy (aCRT) have superior outcomes to the current market CRT devices. The study is seeking participants with heart failure and Left branch bundle block.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Heart failure, Bundle-Branch Block, heart failure, bundle branch block
  • Age: 18 years - 99 years
  • Gender: All
Updated on 19 Feb 2024. Study ID: 820903

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