ICE Based Atrial Flutter Ablation Vs Conventional Fluoroscopy/Anatomical Mapping Based Ablation - ICE Flutter Study
Atrial Flutter
About this trial
This is an interventional treatment trial for Atrial Flutter focused on measuring Atrial Flutter, Ablation, Intra-cardiac echocardiogram (ICE)
Eligibility Criteria
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.
Sites / Locations
- Kansas City Heart Rhythm Institute
- Midwest Heart and Vascular Specialists
- Overland Park Regional Medical Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
3D electroanatomical mapping alone
ICE plus 3D electroanatomical mapping
Patients who are diagnosed with typical right sided flutter who are scheduled for an ablation procedure will be enrolled. Informed consent will be obtained from each of them prior to the procedure. Patients will be randomly assigned to undergo either 3D electroanatomical mapping alone vs ICE plus 3D electroanatomical mapping guided CTI ablation. Operators will plan to alternate each case with the use of ICE + 3D mapping and 3D mapping alone with one method followed by the other for randomization. All patients will have the standard access sheaths placed in the right femoral vein.
Patients who are diagnosed with typical right sided flutter who are scheduled for an ablation procedure will be enrolled. Informed consent will be obtained from each of them prior to the procedure. Patients will be randomly assigned to undergo either 3D electroanatomical mapping alone vs ICE plus 3D electroanatomical mapping guided CTI ablation. Operators will plan to alternate each case with the use of ICE + 3D mapping and 3D mapping alone with one method followed by the other for randomization. All patients will have the standard access sheaths placed in the right femoral vein. The group randomized to ICE catheter placement will have a left femoral 11F sheath placed in addition.