Clinical Trials Directory

Trials / Unknown

UnknownNCT03867266

Typical Atrial Flutter, Ablation Index and Point by Point Ablation

Status
Unknown
Phase
Study type
Observational
Enrollment
400 (estimated)
Sponsor
Ospedale San Francesco · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

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

Detailed description

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.

Conditions

Interventions

TypeNameDescription
PROCEDUREAblation with radiofrequencyAblation point by point on the cavo tricuspid isthmus guided by an index lesion

Timeline

Start date
2019-02-20
Primary completion
2019-06-01
Completion
2019-07-01
First posted
2019-03-07
Last updated
2019-03-07

Locations

1 site across 1 country: Italy

Regulatory

Source: ClinicalTrials.gov record NCT03867266. Inclusion in this directory is not an endorsement.