I48
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Typical (CTI dependent) atrial flutter documented in a standard 12 lead surface ECG with given class I indication for curative CTI ablation according to the current guidelines
Exclusion criteria
Exclusion criteria: previous isthmus ablation, tricuspid valve replacement, bidirectional conduction block not assessable, pregnant or breastfeeding women, abuse of alcohol or drugs
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cumulative ablation duration to bidirectional conduction block | — |
Secondary
| Measure | Time frame |
|---|---|
| - applicated radiofrequency energy to bidirectional conduction block [kJ]; - procedure duration (sheath placement to its removal) [min]; - Efficacy dependent on anatomical factors, such as length and morphology of the CTI; - Efficacy dependent on concomitant diseases, such as diabetes and adiposis; - safety: adverse events; - use of radiation, fluoroscopy time [s], dose area product [cGy*cm^2]; | — |
Countries
Germany
Contacts
Klinikum Fürth, Med. Klinik 1, Kardiologie/Rhythmologie