CompletedNot Applicable

EP Device Registry

Austria, Czechia, France5,003 participantsStarted 2020-06-12

Plain-language 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.

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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.

What they're measuring

The proportion of patients with a device- and/or procedure-related Serious Adverse Event

Timeframe: 7-days

The proportion of procedures that achieved acute success.

Timeframe: Baseline

Trial details

NCT IDNCT04460209

SponsorAbbott Medical Devices

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2026-01-31

View on ClinicalTrials.gov More Cardiac Rhythm Disorder trials