Arrythmia Clinical Trial
Official title:
All Inclusive KODEX - EPD™ Study Patient Specific Optimized Therapy (PSOT) Study
Prospective, multi-center, non-randomized, open label, single arm study. Consented subjects
who are scheduled to undergo ablation due to arrhythmia will be enrolled in the study. Data
will be collected from all subjects during the ablation procedure and post procedure for a
period of 36 months.
KODEX - EPD™ system will be used in all procedures during treatment of cardiac arrhythmias.
Anonymized data will be stored in an EPD database and will be used to train and test
predictors for personalized optimized therapy.
n/a
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