About this trial
Ablation of consecutive atrial tachycardia (AT) after ablation of atrial fibrillation (AF) or cardiac surgery can be challenging due to complex substrate and AT mechanisms. A substantial portion of patients is known to show various tachycardias and recurrences occur in a noticeable number of cases. With the availability of novel ultra-high-density mapping techniques characterization and understanding of AT mechanisms and underlying substrate can be improved. Aim of this prospective, multi-center, randomized study is to compare a standard AT ablation approach versus minimalized ablation of the clinical AT in regards to arrhythmia free survival.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Consecutive AT subsequent to prior AF ablation procedure or cardiac surgery
Surface ECG-documentation of AT as primary clinical arrhythmia
ECG indicating stable, map-able AT (stable activation sequence, and CL stability) with cycle length ≥ 200ms
Disqualifiers
< 18 years
No previous atrial fibrillation ablation procedure or cardiac surgery
Pregnant women or women of childbearing potential without a negative pregnancy test within 48 hours prior to treatment
History of hemorrhagic diathesis or other coagulopathies
Trial design
Parallel
Treatments tested in this trial
Catheter ablation
Procedure/SurgeryCatheter-based ablation of arrhythmias using radiofrequency.
Treatment groups
Trial outcomes
Primary outcomes
Recurrence of any sustained arrhythmia (>30 sec.)
Secondary outcomes
Inducibility of atrial tachycardia (AT) after ablation of clinical/primary AT (partial success)
Categorical variable (yes/no)
Predictability of secondary AT by analysis of clinical AT map and voltage map
Procedure duration time
Fluoroscopy time
Sponsors and contacts
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