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Prospective Procedural Data Collection for Continuous Improvement of the KODEX - EPD™ System Performance.

E

EPD Solutions

Status

Terminated

Conditions

Cardiac Arrhythmia

Treatments

Device: KODEX-EPD system

Study type

Observational

Funder types

Industry

Identifiers

NCT04552665
20-0337

Details and patient eligibility

About

The purpose of the KODEX EPD Field study is to evaluate the performance of the KODEX-EPD system and collect procedural data and medical images for Philips' internal research and development activities (R&D) related to the KODEX-EPD system, as well as for marketing and publication purposes. The KODEX-EPD system is an imaging system that will allow for real time visualization of the catheters in your heart during your procedure, as well as display cardiac images of your heart in several different formats.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cardiac Ablation

Exclusion criteria

  • There is no exclusion criteria

Trial design

30 participants in 1 patient group

Adults
Description:
Patients who have cardiac arrhythmia
Treatment:
Device: KODEX-EPD system

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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