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Recruiting NCT07439016

LA Function After PFA in Paroxysmal AF

Observational Atrial Fibrillation (AF)

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: LA and LAA function measurements.
Who it may be relevant to
Registry conditions: Atrial Fibrillation (AF). 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
Czechia
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

Acute Impairment in Left Atrial and Left Atrial Appendage Function Pre- and Post-Pulse Field Ablation Pulmonary Vein Isolation in Patients With Paroxysmal Atrial Fibrillation: A Prospective Intraprocedural Intracardiac Echocardiography Study

Overview

A prospective study that investigates the changes in LA echocardiographic parameters after PFA for paroxysmal AF.

Detailed description

This study will leverage ICE to define the acute effects of PFA-PVI on LA and LAA function. The findings will deliver pivotal insights into the functional safety of PFA, clarifying whether a transient stunning effect exists and informing the evolution of peri-procedural anticoagulation management.

Research Objectives

Primary Objective:

To quantify the acute changes in LAA mechanical function immediately following PVI using PFA in patients with paroxysmal AF, as assessed by intraprocedural ICE.

Secondary Objectives:

1. To characterize the acute changes in trans-mitral diastolic flow patterns (E velocity, A velocity, E/A ratio, E deceleration time) as surrogate markers of left atrial pressure and compliance following PFA-PVI. 2. To determine the incidence of new-onset LAA functional stunning, defined as a≥20% reduction in LAA ejection fraction (LAA EF) and/or a clinically significant drop in LAA emptying velocity (LAA Ev) compared with baseline. 3. To explore the correlation between pre-procedural LA strain/LAVI measured by TTE and the degree of acute LAA functional impairment post-PFA.

Research Methods

Study Design A prospective, single-center observational study enrolling consecutive patients with symptomatic, drug-refractory paroxysmal AF undergoing first-time PFA-PVI.

Study Population Inclusion criteria: Adults (≥18 years) with paroxysmal AF in sinus rhythm at procedural onset; Exclusion criteria: Persistent or long-standing AF, prior atrial ablation, significant valvular disease, a history of LAA closure Procedural Protocol All PFA procedures will be performed under deep sedation or general anaesthesia using the FARAPULSETM system (Boston Sci.) according to the current recommendations. To measure the LAA and transmitral velocities, an ICE probe will be positioned transeptally into the LA at the beginning and end of the procedure. For this purpose, the transseptal puncture dedicated to the ablation catheter will be utilized; therefore, the study protocol does not require an additional transseptal puncture

PreProcedural TTE:

Comprehensive TTE within 24 hours before ablation will include LVEF, LA volumes, transmitral inflow velocities (E, A), tissue Doppler velocities (e', a'), and advanced strain analysis (reservoir, conduit, contractile strain).

Intra-Procedural ICE:

1. Mitral Inflow Indices: E velocity, A velocity, E/A ratio, and E deceleration time. 2. LAA Functional Indices: LAA emptying velocity (Ev), filling velocity (Fv), maximal area (Amax), minimal area (Amin), and ejection fraction calculated by the area method:

LAA EF = (LAA Amax - LAA Amin) / LAA Amax × 100%. All measurements will be obtained across three cardiac cycles before and within five minutes after completion of PFA PVI.

Endpoints

1. Primary endpoint: Change in LAA EF and LAA Ev between pre- and post- PFA measurements. 2. Secondary endpoints:

* Variation in diastolic indices; * Proportion of patients demonstrating new-onset LAA stunning * correlations with pre-ablation strain/LAVI parameters.

Data Analysis Continuous variables will be summarized as mean ± SD or median (IQR) based on distribution. Pre/post comparisons will use paired t-tests or Wilcoxon signed-rank tests; binary outcomes will employ McNemar's test. Linear regression models will explore relationships between baseline atrial metrics and magnitude of acute functional decline.

Interventions

  • Diagnostic test LA and LAA function measurements
    ICE measurements of the LA and LAA function.

Primary outcome measures

  • 1. Change in LAA Ev between pre- and post- PFA measurements. [Time frame: During the procedure]

Eligibility criteria

Inclusion criteria

  • Age ≥18 years
  • Paroxysmal AF in sinus rhythm at procedural onset

Exclusion criteria

  • Persistent or long-standing AF
  • Prior atrial ablation
  • Significant valvular disease
  • A history of LAA closure

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

Czechia · 1 center
  • University Hospital Kralovske Vinohrady — Prague

Identifiers

NCT: NCT07439016 · LA function PFA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗