Hybrid Ablation Plus Medical Therapy for Persistent Atrial Fibrillation

Status Completed

Clinical Trial Summary

This clinical trial is designed to compare two management strategies for the treatment of asymptomatic/subclinical atrial fibrillation after ablation based on data from the Biotronik ICM (BioMonitor3® or future generation of Biotronik ICM).

Clinical Trial Description

In this study, subjects will be randomized (1:1) to conventional AF management vs. Biotronik ICM-guided AF management following ablation for persistent AF. Subjects will be followed for 15 months including a 3 month blanking period following AF ablation. The study subject population will include subjects with persistent atrial fibrillation (sustained AF episode lasting more than 7 days, but less than 1 year), according to current guideline indications for persistent AF ablation and ICM (Biotronik ICM) implantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04190186
Study type	Interventional
Source	University of Rochester
Contact
Status	Completed
Phase	N/A
Start date	June 25, 2020
Completion date	February 15, 2024

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