AcQMap 2.1 With Electro-Magnetic Tracking System Feasibility Study (EMT Feasibility Study)

Acutus Medical8 enrolled

Overview

Non-Significant Risk Clinical Study Clinical Investigational Use Only for the purposes of collecting electromagnetic tracking data to validate the use of the device in a clinical setting.

The EMT Feasibility Study is a prospective, multi-center, feasibility study designed to demonstrate the feasibility of EMT solution in conjunction with the AcQMap 2.1 System's existing capabilities. The objective of the study is to demonstrate the ability of the AcQMap 2.1 System to support EMT in conjunction with the existing impedance localization capabilities. The new EMT technology is expected to continuously provide fully synchronized and similar localization information to the impedance-based localization information associated with the location of the catheter's magnetic sensor position.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Catheter Ablation

Interventions

The AcQMap 2.1 System with Electro-Magnetic Tracking Feasibility SystemDEVICE

Demonstrate the ability of the AcQMap 2.1 System to support EMT in conjunction with the existing impedance localization capabilities. The new EMT technology is expected to continuously provide fully synchronized and similar localization information to the impedance-based localization information associated with the location of the catheter's magnetic sensor position.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Male or female 18 years of age or older. 2. Currently scheduled for the ablation of an atrial arrhythmia utilizing the diagnostic AcQMap 2.1 System. 3. Willing and able to give written informed consent. Exclusion Criteria: 1. In the opinion of the investigator, any contraindication to the planned ablation, including anticoagulation contraindications, atrial thrombus, renal failure, or sepsis. 2. Current enrollment in any study protocol sponsored by Acutus Medical 3. Any other condition that, in the judgment of the investigator, makes the participant a poor candidate for this procedure, the study, or compliance with the protocol (includes vulnerable patient population, mental illness, addictive disease, extensive travel away from the research center, etc.).

Locations (2)

Kansas City Heart Rhythm Institute

Overland Park, Kansas, United States

Nevada Heart and Vascular

Las Vegas, Nevada, United States

Outcomes

Primary Outcomes

Successful recording of continuous and synchronized impedance and magnetic localization information.

Time frame: Procedure

Data from ClinicalTrials.gov

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