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Implementation of the HELIOSTARTM in Real-world Clinical Practice at a High-volume Center

Atrial Fibrillation Clinical Trial

Official title:
Implementation of the HELIOSTARTM in Real-world Clinical Practice at a High-volume Center - Operator Learning Curve and Procedural Outcome Parameters

Clinical Trial Summary

The HELIOSTARTM catheter (Biosense Webster) is a new technology for pulmonary vein isolation (PVI) in atrial fibrillation (AF), combining radiofrequency (RF)-ablation and 3D-mapping visualization with the concept of "single-shot"-ablation device. This study evaluates the operator learning curve und procedural outcome during implementation of the HELIOSTARTM.

Clinical Trial Description

The first patients undergoing PVI by HELIOSTARTM at Heidelberg University Hospital are included in this prospective study. Procedures are performed by an operator proficient in CB-ablation. Procedural outcome was analyzed over the course of increasing experience with the device and in comparison to a previous cohort investigated during implementation of the Arctic FrontTM-cryoballoon (Medtronic). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05603611
Study type Observational [Patient Registry]
Source University Hospital Heidelberg
Contact
Status Active, not recruiting
Phase
Start date October 26, 2021
Completion date December 30, 2022
View Details
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