Clinical Utility and Validation of the Rhythmia Mapping System for the Treatment of Cardiac Arrhythmias

Completed

• Conditions: Electroanatomic Mapping; Cardiac Arrhythmias; Cardiac Ablation
• Interventions: Device: Rhythmia Mapping System

• Registration Number: NCT03094221
• Lead Sponsor: Beth Israel Deaconess Medical Center

Brief Summary

The purpose of this study is to compare two different types of three-dimensional electroanatomic mapping systems used for the treatment of cardiac arrhythmias. The systems will be compared in regards to its ability to successfully map and ablate a clinical arrhythmia, as well as the time invested in this activity.

Detailed Description

Despite the advancement in catheter ablation technology over the past decade, the essential step in therapy entails identification and accurate mapping of the arrhythmia mechanism and its anatomical substrate. These are performed with the assistance of mapping systems and catheters able to record high fidelity local electrical activity of the heart (electrogram, EGM) and display it in three-dimensional views. Current mapping systems are limited by slow and incomplete arrhythmia mapping, limiting successful therapies.

The Rhythmia™ Mapping System (Rhythmia), including its novel basket catheter (IntellaMap Orion™ High Resolution Mapping Catheter), is an FDA approved mapping system available for use during clinical, standard of care electrophysiology procedures at BIDMC. Its unique design allows improved mapping resolution of cardiac arrhythmias, particularly those with complex disease substrate, such as atrial and ventricular tachycardias. Specifically, the investigators plan to enroll patients undergoing electrophysiology study and ablation for atrial flutter/fibrillation, atrial tachycardia and ventricular tachycardia. The system was developed to provide high-resolution maps based on the rapid, automated acquisition of a very large number of low noise electrograms. This mapping system was designed to improve the speed and clinical outcomes over other systems that do not have this rapid automated acquisition capability.

The Rhythmia mapping system is FDA approved and will be made available for use in clinical procedures at BIDMC. Rhythmia will be installed in one of the three electrophysiology labs at BIDMC and the use of the system is at the discretion of the electrophysiologist performing the procedure. Thus, using or not using the Rhythmia system to guide arrhythmia mapping and ablation is not a deviation from the standard of care.

The goal of this registry study is to examine the clinical utility of the system to create accurate electroanatomical maps and validate the data acquired by comparing it with historical cohorts of electroanatomical signals and their corresponding maps created with the traditional Carto®3 electroanatomic mapping system (Biosense Webster, Inc).

Patients will only be approached for enrollment when the treating physician has elected to utilize the Rhythmia mapping system during the standard clinical procedure. The data acquired will be collected by a member of the research team in a clinical registry for offline analysis.

The aim/hypotheses tested by this study include:

* The Rhythmia mapping system will result in the creation of accurate, high resolution 3D electroanatomical maps, defined as the ability to successfully map the arrhythmia circuit (yes/no) and ablate the arrhythmia (yes/no).

* The time to create an electroanatomical map with the Rhythmia mapping system will be significantly shorter than in historical cohorts using the traditional Carto®3 system.

Study Timeline

• Study Start: 2015-01-13
• Study First Submitted: 2015-10-14
• Primary Completion: 2015-12-01
• Study Completion: 2015-12-01
• Status Verified: 2017-03
• Study First Submitted QC: 2017-03-23
• Last Update Submitted: 2017-03-23
• Study First Posted: 2017-03-29
• Last Update Posted: 2017-03-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Patients above the age of 18 years old.
2. Patients with the diagnosis of atrial or ventricular arrhythmias presenting for electrophysiology study.
3. Patients must be able to understand and critically review the informed consent form.

Exclusion Criteria

1. Patients whom are unable to provide informed consent.
2. Patients with ventricular hypertrophy (LV septum thickness ≥15mm).
3. Patients with prosthetic or stenotic cardiac valves present in the chamber where endocardial mapping is planned
4. Patients with active systemic infections
5. Patients that are pregnant or lactating.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Arrhythmia Mapping	Rhythmia Mapping System	The study sample includes patients referred for three different types of cardiac arrhythmias, which will be the studied categories: 1) atrial flutter/fibrillation, 2) atrial tachycardia, 3) ventricular tachycardia. Patients will undergo standard of care mapping and ablation procedures.

Primary Outcome Measures

Name	Time	Method
Arrhythmia Mapping (Yes/No)	Enrollment (Clinical Procedure)	Ability to successfully map and characterize clinical arrhythmia as confirmed with conventional techniques.
Ablation Success - Elimination of Clinical Arrhythmia (Yes/No)	Enrollment (Clinical Procedure)	Ability to ablate and eliminate the clinical arrhythmia

Secondary Outcome Measures

Name	Time	Method
Mapping Time (minutes)	Enrollment (Clinical Procedure)	Mapping time required to characterize the clinical arrhythmia

Trial Locations

Locations (1)

Beth Israel Deaconess Medical Center; 🇺🇸 Boston, Massachusetts, United States