KODEX – EPD- Patient Specific Optimized Therapy (PSOT) Study
Brief description of study
The
purpose of this research study is to collect data from arrhythmia
patients undergoing catheter-based electrophysiological (EP) intervention (ablation procedures), in which the FDA approved medical device
KODEX-EPD system will be used, in
order to develop a patient specific optimized therapy.
Arrhythmia patients indicated for EP procedures will be recruited from Penn Medicine outpatient and inpatient clinics.
Detailed description of study
If you agree to join the study, you will be
asked to complete the following three follow up visits, at 12 months
post procedure, 24 months post procedure and 36 months post procedure.
These visit can be in-person clinic visit or
by telephone.
Your participation will last about 3 years.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
-
Conditions:
Arrhythmia,indicated for electrophysiological procedures
-
Age: Between 18 Years - 99 Years
-
Gender: All
Updated on
20 Nov 2020.
Study ID: 834416
