The MAGiC™ Cardiac Ablation European Study (MAGiC-FEST)

Stereotaxis

Status

Enrolling

Conditions

Arrhythmias, Cardiac

Treatments

Device: MAGiC™

Study type

Interventional

Funder types

Industry

Other

Identifiers

NCT06019845

MFEAS-001

CIV-23-10-044301 (Other Identifier)

Details and patient eligibility

About

The purpose of the first phase of this feasibility study is to gather safety and performance data on MAGiC to support European marketing approval.

Full description

The purpose of the first phase of this feasibility study is to gather safety and performance data on MAGiC to support European marketing approval. After MAGiC obtains European approval, the study will be amended and expanded to collect Post-Market Clinical Follow-up data.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adult (aged 18 or older at time of consent);
Eligible for ablation procedures of an atrial or ventricular arrhythmia per European Heart Rhythm Association (EHRA) guidelines, with at least one (1) documented episode of the tachyarrhythmia to be treated within the previous six (6) months;
Able to be safely exposed to magnetic fields;
Willing and capable to attend scheduled follow up visits at the investigational site for the study duration (up to 12 months)
Willing and able to provide informed consent.

Exclusion criteria

Unable to be safely exposed to magnetic fields due to Magnetic Resonance Imaging Unsafe device (implanted device or device that cannot be safely removed for the procedure)
Unable to remain comfortable or hemodynamically stable in the supine position for an extended period of time
Weight exceeding 200 kg (the weight limit of the table)
For female patients of childbearing potential: pregnancy at the time of the procedure or unwilling to take a pregnancy test
Presence of intracardiac thrombus at the time of the procedure
Where MAGiC would need to cross a prosthetic valve
Use of MAGiC in the coronary arteries
A history of sensitivity to foreign objects or extreme allergies
Acute illness or active systemic infection
Histological or anatomical abnormalities that may lead to post-operative complications including diminished resistance to infection
Hemodynamic instability
Unable to receive heparin or an acceptable alternative to achieve adequate anticoagulation
Acute myocardial infarct (within the previous 30 days)
Recent cardiac surgery (within the previous 60 days)
Unstable angina
History of embolism (cerebrovascular accident, transient ischemic attack, systemic embolism) in the previous 30 days
Previous cardiac ablation within the previous 30 days
Concomitant arrhythmia(s) requiring active treatment at this time or in the 90 days prior to enrollment (Day -90 to Day 0)
Currently or in the 30 days prior to consent, participation in an interventional clinical trial
Significant uncontrolled or unstable medical problems which, in the opinion of the Investigator, would preclude enrollment in and completion of the study (limitation on survival).
Any reason or condition that, in the judgement of the investigator, makes the patient ineligible for the investigation.
For Atrial Fibrillation only: persistent Atrial Fibrillation (continuous Atrial Fibrillation lasting longer than 7 days)
For Atrial Fibrillation only: Presence of any device that would interfere with planned access: Patent Foramen Ovale occlusion/closure device, patch