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PULSED AF (Atrial Fibrillation) - Clinical Trial

What is the Purpose of this Study?

We are doing this study to collect information about the clinical performance of the PulseSelect® Pulsed Field Ablation (PFA) System. The PFA system was recently approved by the FDA as a treatment for both paroxysmal and persistent atrial fibrillation (AF). We want to learn more about how well it works for AF patients now that it is a widely available option. We will assess how well it improves symptoms for people who who have persistent AF that has lasted less than one year, or have experienced episodes of paroxysmal atrial fibrillation, or have persistent or paroxysmal atrial fibrillation that is not controlled by medication, or have symptoms from their persistent or paroxysmal atrial fibrillation.

What is the Condition Being Studied?

Atrial Fibrillation (AF)

Who Can Participate in the Study?

Adults ages 18+ who:

  • Are diagnosed with recurrent symptomatic paroxysmal AF or persistent AF
  • Cannot be treated with at least one Class I or III antiarrhythmic drug (i.e., not effective, not tolerated, or not desired)
  • Are planning to have a pulmonary vein isolation procedure with the PulseSelect® PFA System

For more information, contact the study team at jessalyn.crews@duke.edu.

Grupo etario
Adultos

What is Involved?

If you choose to join this study, the study doctor and study coordinator will collect information about you and your medical history, including medications that you are currently taking or recently used. You will be considered enrolled in the study once you sign the consent form before your planned procedure. None of the procedures in this study are experimental.

You will visit the study team at the following times during the study:

  • On the day of enrollment when you sign the study's consent form
  • The day of your ablation procedure
  • 3 months after your ablation procedure
  • 6 months after your ablation procedure
  • 1 year after your ablation procedure
  • 2 years after your ablation procedure
  • 3 years after your ablation procedure

The 6 month and the 1 year follow-up visits will need to be in our clinic, but the rest of the visits can be done remotely (over the phone).

Study Details

Full Title
PULSED AF Post-Approval Study, an Addendum to the PulseSelect™ PFA Global Registry
Principal Investigator
Especialista en electrofisiología
Protocol Number
IRB: PRO00117351
NCT: NCT06578104
Phase
Phase IV
ClinicalTrials.gov
Estado de inscripción
Pronto disponible para inscripción