Atrial Fibrillation (AF)NCT07439016
LA Function After PFA in Paroxysmal AF
An observational study of Atrial Fibrillation (AF), run by Charles University, Czech Republic at 1 site in Czechia.
Trial summary
A prospective study that investigates the changes in LA echocardiographic parameters after PFA for paroxysmal AF. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Atrial Fibrillation (AF)
- What is being tested?
- LA and LAA function measurements
- How many people
- 50 participants
- Where
- 1 siteCzechia
- Study dates
- 1 Nov 2025to 1 Nov 2026
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients scheduled for AF ablation.
Who may be able to join
- Age ≥18 years
- Paroxysmal AF in sinus rhythm at procedural onset
Who cannot join
- Persistent or long-standing AF
- Prior atrial ablation
- Significant valvular disease
- A history of LAA closure
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Czechia1 site, 1 recruiting
- Recruiting
University Hospital Kralovske Vinohrady
Prague
About this study
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
A prospective study that investigates the changes in LA echocardiographic parameters after PFA for paroxysmal AF.
Read the 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:
- 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.
- 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.
- 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:
- Mitral Inflow Indices: E velocity, A velocity, E/A ratio, and E deceleration time.
- 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
- Primary endpoint: Change in LAA EF and LAA Ev between pre- and post- PFA measurements.
- 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.
- Conditions
- Atrial Fibrillation (AF)
- Being tested
- LA and LAA function measurements
- Keywords
- atrial fibrillation, catheter ablation, LA function
- Medical subject headings
- Atrial Fibrillation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
LA and LAA function measurementsDiagnostic test
ICE measurements of the LA and LAA function.
| Study group | Role | What they receive |
|---|---|---|
| Cohort 1 | Measurement of the LA and LAA echocardiographic parameters pre- and post-PFA for paroxysmal AF. Receives: Diagnostic Test: LA and LAA function measurements |
What is being measured
The primary outcome is the main question the study is designed to answer.
1. Change in LAA Ev between pre- and post- PFA measurements.
Measured: During the procedure
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted27 Feb 2026
- Study start1 Nov 2025
- Primary completion1 Nov 2026 (estimated)
- Study completion1 Nov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Atrial Fibrillation (AF)Studies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Charles University, Czech Republic
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Marek Hozman, MD, PhD, Charles University, Czech Republic
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07439016
- Sponsor's protocol ID
- LA function PFA
- Status last verified
- Mar 2026
- First submitted
- 19 Nov 2025
- Last updated
- 18 Mar 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 18 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT07439016
- Acronym / sponsor ID
- LA function PFA
- Conditions
- Atrial Fibrillation (AF)
- Keywords
- atrial fibrillation, catheter ablation, LA function
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Charles University, Czech RepublicUniversity, hospital or other
- Study start
- 1 Nov 2025 (actual)
- Primary completion
- 1 Nov 2026 (estimated)
- Study completion
- 1 Nov 2026 (estimated)
- First posted
- 27 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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:
- 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.
- 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.
- 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:
- Mitral Inflow Indices: E velocity, A velocity, E/A ratio, and E deceleration time.
- 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
- Primary endpoint: Change in LAA EF and LAA Ev between pre- and post- PFA measurements.
- 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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cohort 1 | – | Diagnostic Test: LA and LAA function measurementsMeasurement of the LA and LAA echocardiographic parameters pre- and post-PFA for paroxysmal AF. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients scheduled for AF ablation.
Key inclusion criteria (2 listed)
- Age ≥18 years
- Paroxysmal AF in sinus rhythm at procedural onset
Key exclusion criteria (4 listed)
- Persistent or long-standing AF
- Prior atrial ablation
- Significant valvular disease
- A history of LAA closure
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LA and LAA function measurementsICE measurements of the LA and LAA function. | Diagnostic test | Cohort 1 |
Primary outcome
1. Change in LAA Ev between pre- and post- PFA measurements.
Time frame: During the procedure
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 18 Mar 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Atrial Fibrillation (AF), run by Charles University, Czech Republic at 1 site in Czechia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 18 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Czechia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Marek Hozman, MD, PhD (+420267161111, marek.hozman@fnkv.cz), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
1. Change in LAA Ev between pre- and post- PFA measurements. (time frame: During the procedure). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Mar 2026.