PULSED AF Post-Approval Study

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorMedtronic Cardiac Ablation Solutions

About this trial

PULSED AF PAS is a prospective, global, multi-center, non-randomized, observational trial. Subjects will be treated with the PulseSelect™ PFA System and followed through 36 months.

Eligibility criteria

Qualifiers

A diagnosis of recurrent symptomatic paroxysmal AF or persistent AF

Refractory to at least one Class I or III antiarrhythmic drug (i.e., not effective, not tolerated, or not desired)

Patient is ≥ 18 years of age

Planned pulmonary vein isolation procedure with the commercially available PulseSelect™ PFA System

Disqualifiers

Long-standing persistent AF (continuous AF sustained >12 months)

Prior left atrial catheter or surgical ablation

Patient with life expectancy < 36 months

Presence of a permanent pacemaker, biventricular pacemaker, loop recorder/insertable cardiac monitor (ICM), or any type of implantable cardiac defibrillator (with or without biventricular pacing function)

Trial design

Treatments tested in this trial

  • PulseSelect™ PFA system

Treatment groups

580 Participants
are divided into 2 treatment groups