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AF-FLOW Registry: This Study is to Evaluate Ablamap Software in Patients Undergoing Ablation for Atrial Fibrillation.

Cardiovascular Diseases Clinical Trial

Official title:
A Post Market, Global Registry to Evaluate the Identification of Atrial Fibrillation Sources Using the Ablamap® Electrographic FLOW (EGF) Mapping System to Guide Ablation Therapy in Patients With Atrial Fibrillation

Clinical Trial Summary

This post-market global registry will evaluate the ability of the Ablamap® Software to identify atrial fibrillation sources and guide ablation therapy in patients with atrial fibrillation.

Clinical Trial Description

The AF-FLOW Registry is a prospective, multi-center global post-market registry that will obtain clinical data in order to characterize the performance of the Ablamap® Software for its intended use in a real-world setting. Specifically, we will evaluate the ability of the Ablamap® Software to identify AF sources and guide ablation therapy in patients with atrial fibrillation. This registry will enroll up to 100 subjects. Subjects that present with atrial fibrillation and meet inclusion/exclusion criteria will be eligible for enrollment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05481359
Study type Observational [Patient Registry]
Source Ablacon, Inc.
Contact
Status Active, not recruiting
Phase
Start date September 12, 2022
Completion date December 2023
View Details
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