ICE Based Atrial Flutter Ablation Vs Conventional Fluoroscopy/Anatomical Mapping Based Ablation - ICE Flutter Study
Sponsored by Kansas City Heart Rhythm Research Foundation
About this trial
Last updated 3 years ago
Study ID
Status
Type
Phase
Placebo
Accepting
Not accepting
Trial Timing
Ended 3 years ago
What is this trial about?
What are the participation requirements?
Inclusion Criteria
All patients undergoing typical CTI dependent AFL who give informed consent for participation in the study will be included.
Exclusion Criteria
- Patients in whom placement of an ICE catheter in the right atrium for adequate atrial visualization is technically not feasible. - Patients who cannot give an informed consent will be excluded. - Patients in who vascular access for the 11F sheath is not feasible will be excluded. Those with left iliac vein stenosis or left groin arteriovenous (AV) fistulas or prior left groin access complications will be excluded. - Patients who on the EP (Electrophysiology) study are found to have a left sided arrhythmia needing transseptal access will be excluded. - Patients who during EP study are found to have atypical flutter pathways including Left Atrial (LA)/Left sided flutter as above, atypical pathways outside of the CTI, and scar based- reentry pathways.