This pilot, prospective, interventional, monocentric, independent, and no-profit clinical trial aims to investigate and evaluate the proportion, acute and chronic characteristics, and outcomes of esophageal thermal injury (ETI) in AF ablation using a high-power, short-duration (HP-SD) setting with contact force (CF) sensing tip ablation catheter in standard clinical practice. The main questions it aims to answer are: * Evaluate the acute proportion of the ETI assessed by the mini-invasive esophagoscopy pre and post-procedure. In addition, clinical evaluations at 3, 6, and 12 months from the procedure are foreseen. * Evaluate the contribution of the factors influencing RF procedure (contact force, impedance, RF power, RF time) on ETI development. * Describe the relationship between the esophageal temperature (continuous monitoring) and ETI development.
This study aims to estimate the proportion of esophageal thermal injury (ETI) as a result of the AF ablation using a high-power, short-duration (HP-SD) setting with contact force (CF) sensing tip ablation catheter immediately after and at 3, 6, and 12 months from the procedure, as well as describe their characteristics. To be more sensitive and specific in detecting the presence of potentially chronic and progressing ETIs in esophageal ulcers and atrium-esophageal fistula, a minimally invasive esophagogastroscope will be used before (1-7 days) and after (1-3 days) the ablation procedure, with an internal comparison of the lesions observed. In addition, various clinical characteristics of the patients and descriptors of the ablation procedure (such as contact force, impedance, RF power, RF time, esophageal temperature, procedure times, etc.) will be collected and related to the presence of ETI. The principal Medical Devices that will be used: 1. Cardiac Mapping system Ensite X (Abbott Medical), 2. Tip CF sensing catheter TactiFlex (Abbott Medical), 3. High mapping density catheter (HD GRID/Advisor FL, Abbott Medical), 4. Continuous temperature monitoring devices (Esotest Multi/Esotherm 7 poles, FIAB), 5. Video-endoscope EXERA III HDTV dual focus GIF-HQ190 (Olympus).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
PREVENTION
Masking
NONE
Enrollment
51
mini-invasive esophagoscopy assessment of esophageal thermal injury (ETI) after an AF ablation session in an HP-SD setting, and with a tip CF sensing ablation catheter
AF ablation session in an HP-SD setting and with a tip CF sensing ablation catheter
SOD di Cardiologia e Aritmologia
Ancona, Italy
RECRUITINGProportion of the acute esophageal thermal injury (ETI)
Evaluate the acute proportion of the esophageal thermal injury (ETI)
Time frame: 1-3 days after AF ablation procedure
Factors influencing RF procedure on ETI development
Contribution of the factors influencing RF procedure (contact force, impedance, RF power, RF time) on ETI development
Time frame: 1-3 days after AF ablation procedure
Esophageal temperature by an esophageal continuous monitoring device
Celsius degree.
Time frame: during AF ablation procedure
ETI monitoring
Chronic (every 3 months until healing) evaluation of discovered ETI.
Time frame: 12 months after AF ablation procedure
AF ablation procedure times
minutes
Time frame: 1 day
AF recurrences
AF recurrences until 12 months after the ablation procedure
Time frame: 12 months after AF ablation procedure
Serious and no serious adverse events
Serious and no serious adverse events after the ablation procedure
Time frame: 12 months after AF ablation procedure
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