The MAGiC™ Cardiac Ablation European Study

NCT ID: NCT06019845

Last Updated: 2025-05-13

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 150 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-02
• Study Completion Date: 2026-09-30

Brief Summary

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

Detailed 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.

Conditions

Arrhythmias, Cardiac

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

Magnetic Interventional Ablation Catheter (MAGiC™)

Group Type: EXPERIMENTAL

MAGiC™

Intervention Type: DEVICE

Robotic magnetic radiofrequency (RF) ablation catheter

Interventions

MAGiC™

Robotic magnetic radiofrequency (RF) ablation catheter

Intervention Type: DEVICE

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Osypka AG

UNKNOWN

Sponsor Role: collaborator

Stereotaxis

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Betsy Lowry

Role: STUDY_DIRECTOR

Stereotaxis

Locations

Rigshospitalet, University of Copenhagen

Copenhagen, , Denmark

Site Status: RECRUITING

Vilniaus universiteto ligoninė Santaros klinikos

Vilnius, , Lithuania

Site Status: RECRUITING

Countries

Denmark; Lithuania

Central Contacts

Betsy Lowry

Role: CONTACT

betsy.lowry@stereotaxis.com

9737236613

Facility Contacts

Aslaug Karlsdóttir

Role: primary

aslaug.thora.karlsdottir@regionh.dk

Lærke Bjerregaard Heidum

Role: backup

laerke.bjerregaard.heidum@regionh.dk

Kridtina Ščerbakovaitė

Role: primary

Kristina.Scerbakovaite@santa.lt

Jūratė Barysienė

Role: backup

Jurate.Barysiene@santa.lt

Other Identifiers

CIV-23-10-044301

Identifier Type: OTHER

Identifier Source: secondary_id

MFEAS-001

Identifier Type: -

Identifier Source: org_study_id