Dielectric Tissue Imaging in Cavotriscuspid Isthmus Ablation
Brief description of study
The purpose of this research study is to collect data from arrhythmia patients undergoing catheter-based ablation of the cavotricuspid isthmus using the Food and Drug Administration (FDA) cleared medical device KODEX - EPD™. This is an imaging system that will allow for real time visualization of the catheters in your heart during your procedure, as well as display cardiac images of your heart in several different formats. The study team will gather data and physician input for the further development of the KODEX – EPD™ functions for assessing tissue properties to learn how to improve future patients’ arrhythmia treatment.
Clinical Study Identifier: s19-01938
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