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Study identifier: NCT04750798 Synced from ClinicalTrials.gov · August 03, 2026
● Recruiting

An Observational Post-marketing Study Using Commercially Approved Biosense Webster (BWI) Medical Devices for the Treatment of Participants With Cardiac Arrhythmias

Condition: Arrhythmias, Cardiac  ·  Sponsor: Biosense Webster, Inc.

PhaseN/A
Planned participants8000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to prospectively collect clinical data evaluating the ongoing safety and performance during routine-use standard cardiac arrhythmia mapping and/or ablation procedures while using commercial Biosense Webster Inc. (BWI) medical devices. Data generated from the study will be used to confirm safety and performance of BWI medical devices in the marketed phase and to expand the body of evidence on the use of these devices and techniques in treatment of cardiac arrhythmias.

This description comes directly from the study's public registry record.

Talk to the study team

Nathalie Macours  ·  +32 479 97 05 05  ·  nmacours1@its.jnj.com

Liesbeth Gorissen  ·  LGORISSE@ITS.JNJ.com

Always discuss trial participation with your own doctor first.

Locations (41)

Medical University of GrazGraz, AustriaRecruiting
Ordensklinikum Linz GMBHLinz, AustriaRecruiting
Universitätsklinikum Wiener NeustadtWiener Neustadt, AustriaRecruiting
OLV AalstAalst, BelgiumRecruiting
AZ Sint-Jan BruggeBruges, BelgiumRecruiting
CHU Saint-PierreBrussels, BelgiumRecruiting
UZ AntwerpEdegem, BelgiumRecruiting
Jessa HospitalHasselt, BelgiumRecruiting
UZ BrusselsJette, BelgiumRecruiting
ASBL CHU HELORA Hôpital de La Louvière site JolimontLa Louvière, BelgiumRecruiting
Aarhus University HospitalAarhus, DenmarkRecruiting
RigshospitaletCopenhagen, DenmarkRecruiting

+ 29 more locations — full list on the registry record.

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