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Prospective Registry on User Experience With The Mapping System For Ablation Procedures — TRUE-HD  

Cardiac Arrhythmias Clinical Trial

Official title:
Prospective Registry on User Experience With The Mapping System For Ablation Procedures

Clinical Trial Summary

This is an observational, prospective, non-randomized, multicenter, post approval study being conducted in the United States, Europe and Asia-Pacific Regions.

Clinical Trial Description

The TRUE HD Study is aimed at collecting real-world data on the use of the Rhythmia mapping system and the IntellaMap Orion mapping catheter in patients indicated for ablation procedure with use of a 3D Mapping system.

The study will collect specific information on management of ablation procedures with the commercial system including but not limited to acute procedural success, type and proportion of arrhythmias mapped/treated, and how mapping system is used overall. Usage data may be used for the planning of future clinical trials. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02698670
Study type Observational [Patient Registry]
Source Boston Scientific Corporation
Contact
Status Completed
Phase N/A
Start date May 25, 2016
Completion date May 2017
View Details
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