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The aim is to use the Advisor™ HD Grid Mapping Catheter, Sensor Enabled™ to characterize the atrial substrate and develop a model for predicting recurrence rates after a single procedure using a PVI only approach and a contact catheter.
This clinical investigation is intended to characterize the left atrial substrate using the Advisor™ HD Grid Mapping Catheter, Sensor Enabled™ in an HD Wave configuration and correlate different factors with 12-month success after a single ablation procedure using a pulmonary vein isolation (PVI) approach without further substrate modification. This is a post-market, single-arm, multi-center, prospective interventional study of the Advisor™ HD Grid Mapping Catheter, Sensor Enabled™. This study is aimed at determining correlations between pre-ablation mapping characteristics and outcomes after catheter ablation of atrial fibrillation. Approximately 300 subjects at up to 20 sites worldwide will be enrolled. Subjects will be followed until they complete their 12-month visit. Clinical Investigation visits will occur at Baseline (confirmation of eligibility), Index Procedure, 3 months, 6 months, and 12 months. Endpoints will be analyzed when all subjects have completed their 12-month follow up visits.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Kepler Universitätsklinikum GmbH
Linz, UPR AUS, Austria
FN U sv. Anny v Brno
Brno, Moravia-Silesia, Czechia
CHR de La Reunion - Site du CHFG
Saint-Denis, ILE, France
Hôpital Privé du Confluent
Nantes, Paysdel, France
Médipôle Lyon-Villeurbanne
Villeurbanne, Rhone, France
Klinikum Ingolstadt GmbH
Ingolstadt, Bavaria, Germany
Herz- u. Gefäßzentrum Bad Bevensen
Bad Bevensen, L Saxon, Germany
Herz- und Diabeteszentrum NRW
Bad Oeynhausen, Germany
Ospedale San Raffaele
Milan, Lombard, Italy
Azienda Ospedaliero Universitaria Pisana
Pisa, Tuscany, Italy
Start Date
August 26, 2019
Primary Completion Date
November 30, 2021
Completion Date
January 13, 2022
Last Updated
September 19, 2024
300
ACTUAL participants
A specific electrophysiology mapping protocol is applicable with the GRID catheter.
PROCEDURE
Lead Sponsor
Abbott Medical Devices
NCT03546374
NCT07301190
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07281898