University Hospital Kralovske Vinohrady
Prague, Czechia
Location status: Recruiting
NCT Number: NCT07439016
A prospective study that investigates the changes in LA echocardiographic parameters after PFA for paroxysmal AF.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Prague, Czechia
Location status: Recruiting
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:
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:
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
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
ICE measurements of the LA and LAA function.
Time frame: During the procedure
Contact information is provided by the study sponsor or research team.
Charles University, Czech Republic
Other
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
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07728539
Acute Cerebrovascular Accident, Arrhythmias, Cardiac
Moscow, Russia
View Trial DetailsNCT07726056
Arrhythmias, Cardiac, Atrial Fibrillation
Melbourne, Australia
View Trial DetailsNCT07724899
Arrhythmias, Cardiac, Atrial Fibrillation
Chengdu, Sichuan, China
View Trial DetailsNCT07175428
Arrhythmias, Cardiac, Atrial Fibrillation
Dothan, Alabama, United States
View Trial Details