AdaptResponse Clinical Investigation Plan

AdaptResponse Clinical Investigation Plan

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: Between 18 Years - 99 Years
  • Gender: All
Updated on 07 Sep 2022. Study ID: 820903

Interested in the study

Select a study center that’s convenient for you, and get in touch with the study team.

Contact a study center