MedPath

EP Device Registry

Recruiting
Conditions
Cardiac Rhythm Disorder
Registration Number
NCT04460209
Lead Sponsor
Abbott Medical Devices
Brief Summary

This study will provide ongoing, high quality data on the safety, performance, and clinical benefits of Abbott's EP devices in a real-world setting.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
7500
Inclusion Criteria
  • Subject underwent an electrophysiology imaging (diagnostic procedure) and/or ablation procedure that used one or more Abbott devices covered by this Registry.
  • Subject is willing and able to comply with the site's standard of care follow-up schedule.
Exclusion Criteria
  • Subject is currently participating in another clinical investigation that may confound the results of this Registry.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The proportion of patients with a device- and/or procedure-related Serious Adverse Event7-days

that occurred within 7-days of the procedure.

The proportion of procedures that achieved acute success.Baseline
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (26)

KH Wiener Neustadt

🇦🇹

Wiener Neustadt, Lower Austria, Austria

A. ö. Krankenhaus der Elisabethinen Linz

🇦🇹

Linz, Upr Aus, Austria

FN U sv. Anny v Brno

🇨🇿

Brno, Moravia-Silesia, Czechia

Pole Sante Republique

🇫🇷

Clermont-Ferrand, Auvergne, France

Polyclinique des Fleurs

🇫🇷

Ollioules, Provence-Alpes-Azur, France

Clinique Rhône-Durance

🇫🇷

Avignon, Provence, France

Deutsches Herzzentrum München des Freistaates Bayern

🇩🇪

München, Bavaria, Germany

Medizinische Einrichtungen der Universität zu Köln

🇩🇪

Köln, North Rhine-Westphalia, Germany

Herzzentrum Dresden GmbH Universitätsklinik

🇩🇪

Dresde, Germany

Semmelweis University

🇭🇺

Budapest, Hungary

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KH Wiener Neustadt
🇦🇹Wiener Neustadt, Lower Austria, Austria
Christina Mayr
Contact
christina.mayr@wienerneustadt.lknoe.at

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