Typical Atrial Flutter Clinical Trial
Official title:
Typical Atrial Flutter, Ablation Index and Point by Point Ablation
The Ablation of the typical atrial flutter can be considered substantially anatomical, the investigators want to test a protocol that foresees the use a lesion index (AI) and that respects the Inter-Lesion Distance (ILD) ≤ 6 mm on the cavo-tricuspid isthmus (CTI) The investigators want to prove how the introduction of a lesion index combined with the continuity of lesion can allow a "first pass block" of the CTI decreasing total Radio-Frequency (RF) times
The Ablation of the typical atrial flutter can be considered substantially anatomical, the
aim of the study is to test a protocol that foresees the use a lesion index and that respects
the Inter-Lesion Distance ≤ 6 mm on the cavo-tricuspid isthmus to prove how the introduction
of a lesion index combined with the continuity of lesion can allow a "first pass block" of
the CTI decreasing total Radio-Frequency times With the aim of reducing the use of the
fluoroscopy and ionizing radiations, an anatomical map of the right atrium will be
reconstructed with a mapping catheter in all patients, and a 10-pole catheter will be placed
in the coronary sinus.Then, the anatomy of the isthmus will be precisely defined with a
catheter equipped with a force sensor ,identifying the tricuspid valve as the initial point
of ablation and the inferior vena cava- right atrium junction as the end point of the
line.Once the reconstruction has been completed, the ablation phase will start. Considering
the values already validated for the left atrium, the protocol foresees the point-by-point
ablation with the use of AI ≥ 500 and ILD≤ 6 mm.
The Visitag setting will be the following:
- Respiration Adjustment;
- Catheter Position Stability Min. Time = 3 sec, Max. Range = 5 mm;
- Force Over Time Time = 30% Min. Force = 4 gr. The power can be set between 35 and 40
watts. At the end of the isthmus ablation, line block will be evaluated by proximal CS
pacing, acquiring at least 3 distinct points from the ablator catheter around the
tricuspid annulus ,typically ostium of coronary sinus (CS), lateral tricuspid annulus
and a point more proximal to the line of ablation.
Once this phase has been completed, 20 minutes of waiting time has to be considered. After
this waiting time the block of the isthmus will be validated again with the same protocol
described above.
Primary Endpoint -Anatomical first Pass block of the CTI.
Secondary Endpoint
-Reduction of procedural, RF and fluoroscopy times.
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