CellFX nsPFA Cardiac Surgery System to Treat Atrial Fibrillation (NANOCLAMP AF STUDY) - Clinical Trial

¿Cuál es el Propósito de este estudio?

In this study, you will have a heart procedure called an ablation using a special system called the nsPFA Cardiac Surgery System. After the procedure, you will have follow up visits at one month, three months, six months, and twelve months. Around each visit, you will wear a heart monitor to track your heart rhythm and use a phone app to share information. The study team will also collect information about your medicines and your health during the study.

¿Cuál es la Condición que se está estudiando?

Fibrilación auricular

¿Quién puede participar en el Estudio?

People can join this study if they have had atrial fibrillation and are scheduled to have planned heart surgery that is not an emergency. They cannot join if they have a pacemaker, an artificial heart valve, kidney failure, or a long term lung disease called chronic obstructive pulmonary disease.

Grupo etario
Adultos

¿Qué Implica?

The purpose of this study is to find out if a medical system called the CellFX nsPFA Cardiac Surgery System is safe and works well to treat a heart rhythm problem called atrial fibrillation. Researchers want to learn how well this system helps fix the irregular heartbeat and keeps patients safe during and after treatment.

Detalles del Estudio

Título Completo
Pulse Biosciences' CellFX nanosecond Pulsed Field Ablation (nsPFA) Cardiac Surgery Clamp System for treatment of Atrial Fibrillation (AF) during concomitant cardiac surgery
Investigador Principal
Adam Williams, MD
Especialista en cirugía cardíaca
Número de Protocolo
IRB: PRO00119255
Fase
Fase N/A
Estado de inscripción
Abierto para inscripción
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Contribuya a Duke Health