Atrial Fibrillation Clinical Trials

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Evaluation of the Efficacy of Pulmonary Vein Isolation by Pulsed-field Ablation in Persistent Atrial Fibrillation: a Multicenter Study With Follow-up by Implantable Cardiac Monitor

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Atrial fibrillation (AF) is the most common sustained arrhythmia in adult population. According to current guidelines for the management of AF, radiofrequency (RF) ablation (including at least pulmonary vein isolation \[PVI\]) is a validated therapeutic option for persistent AF. Recently, Pulsed-field ablation (PFA) - a new non-thermal energy - has been used to treat paroxysmal and persistent AF with a high success rate in observational studies. This new technology is based on tissue-specificity on myocardium, avoiding collateral damages on adjacent structures. Before confirming a superiority of PFA over existing thermal energies, prospective studies concerning an exclusive population of persistent AF patients are needed, with rigorous assessment of the recurrences using continuous monitoring (insertable cardiac monitor \[ICM\]). PFA efficacy using ICM has never been evaluated. Before considering PFA in therapeutic strategies through large-scale randomized studies using rigorous monitoring of recurrences, preliminary studies are needed in a persistent AF population-only. This pilot cohort study will provide solid data of PFA efficacy (using continuous monitoring of recurrences) for future randomized studies.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Symptomatic persistent AF (continuous episode sustained beyond 7 days)

• Refractory, intolerant or unwilling to take ADT

• Signed informed consent

• Affiliation to medical social coverage.

⁃ Non inclusion Criteria:

• Persistent long-term atrial fibrillation with ongoing episode continuous for more than 3 years;

• Left ventricular ejection fraction ≤ 15% ;

• Stage IV of the New York Heart Association classification;

• Previous atrial ablation outside the cavotricuspid isthmus;

• Wearer of an implantable electronic cardiac prosthesis (pacemaker or defibrillator; MCI)

• Hypertrophic heart disease other than hypertensive hypertrophic heart disease;

• Severe valvular heart disease, including the presence of a mechanical mitral valve or any mitral surgery;

• Congenital heart disease, including atrial septal defect, patent foramen ovale treated by percutaneous closure with atrial septal prosthesis;

• Presence of cardiac thrombus;

• Myocardial infarction or percutaneous coronary angioplasty within the last 6 months;

• Cardiac surgery within the last 6 months;

• Systemic thromboembolic event less than 6 months ago;

• Pulmonary embolism less than 6 months ago or pulmonary hypertension requiring specific treatment;

• Inability to read independently

• Vulnerable patient: minor, patient under curatorship or guardianship

Locations
Other Locations
France
CHU de Nice
RECRUITING
Nice
Contact Information
Primary
Sok-Sithikun BUN, MD, PhD
bun.s@chu-nice.fr
04 92 03 77 33
Backup
Laura VIALE-TRIGLIA
viale-triglia.l@chu-nice.fr
04 92 03 24 46
Time Frame
Start Date: 2026-04-13
Estimated Completion Date: 2030-04-13
Participants
Target number of participants: 60
Treatments
Experimental: Symptomatic persistent atrial fibrillation
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Universitaire de Nice

This content was sourced from clinicaltrials.gov