Menu
Recruiting NCT07353775

Intracardiac Echocardiography-Guided Cavotricuspid Isthmus Ablation With a Circular-Shaped Pulsed Field Ablation Catheter

Observational Atrial Fibrillation (AF) Atrial Flutter

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: ICE-guided CTI ablation with PFA.
Who it may be relevant to
Registry conditions: Atrial Fibrillation (AF), Atrial Flutter. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Intracardiac Echocardiography-Guided Cavotricuspid Isthmus Ablation With a Circular-Shaped Pulsed Field Ablation Catheter: A Prospective Study on Effectiveness and Safety

Overview

This observational study aims to evaluate the effectiveness and safety of a circular-shaped pulsed field ablation (PFA) catheter for CTI ablation under the guidance of intracardiac echocardiography (ICE). The main question it aims to answer is: Is the circular-shaped PFA catheter an effective and safe tool for achieving acute success for CTI ablation? Patients undergoing CTI ablation with a circular-shaped PFA catheter will be prospectively enrolled.

Interventions

  • Procedure ICE-guided CTI ablation with PFA
    Cavotricuspid isthmus ablation with a circular-shaped pulsed field ablation catheter guided by intracardiac echocardiography

Primary outcome measures

  • Acute Success of CTI Block [Time frame: Within the ablation procedure]
Secondary outcome measures (5)
  • CTI Procedural Time [Time frame: Within the ablation procedure]
  • Total PF Application Time [Time frame: Within the ablation procedure]
  • Number of PFA Applications [Time frame: Within the ablation procedure]
  • Procedure-related Complications [Time frame: Within 30 days after the ablation procedure]
  • Freedom from Any Atrial Arrhythmia [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Paroxysmal or persistent atrial fibrillation
  • Aged 18 years or older
  • Scheduled for CTI ablation
  • Able and willing to provide written informed consent

Exclusion criteria

  • Previous CTI ablation
  • Significant congenital heart disease or structural anomaly affecting the CTI
  • Active intracardiac thrombus
  • Pregnancy or lactation
  • Severe renal/hepatic insufficiency
  • Active systemic infection or sepsis
  • Life expectancy of less than 12 months
  • Unable to provide written informed consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Beijing Anzhen Hospital — Beijing

Identifiers

NCT: NCT07353775 · PFA-CTI ablation

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗