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Clinical Trial Summary

The goal of this registry/observational study is to collect data on the clinical utility of MediGuide™ system in cardiac resynchronization therapy (CRT) implantation and electrophysiology (EP) procedures.


Clinical Trial Description

The intent of this worldwide registry/observational study is to understand the utility of the MediGuide™ technology in real world clinical practice during CRT implantation and study-specific-EP procedures. The study should provide an understanding of the effect of MediGuide™ technology on:

- The amount of fluoroscopy time and the radiation exposure

- Total procedure time

- Peri-procedural clinical event rate

Additionally, this study will address the following

- Identification of procedural challenges which may aid in developing future MediGuide tools

- Evaluation of newly available MediGuide tools during the study

- Correlation between MediGuide operator experience and the radiation exposure amount and time ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02470312
Study type Observational [Patient Registry]
Source Abbott Medical Devices
Contact
Status Terminated
Phase
Start date August 18, 2015
Completion date February 28, 2018

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