Magnetic heart fix: new device targets dangerous rhythms
NCT ID NCT06019845
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new device called MAGiC that uses magnets to help doctors treat abnormal heart rhythms. About 150 adults who need a standard heart ablation procedure will take part. The goal is to see if the device is safe and works well, both right after the procedure and over the next year.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2024
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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, lctrocardiographically documented within 12 months \[rior to enrollment; * Able to be safely exposed to magnetic fields; * Willing and capable to attend scheduled follow up visits at the study 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) * Women of childbearing age who are pregnant or who plan to become pregnant within the course of their participation in the study. Must have a negative pregnancy test. * Presence of intracardiac thrombus within 12 weeks prior to enrollment * 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 * Unable to receive heparin or an acceptable alternative to achieve adequate anticoagulation * Acute myocardial infarct (within the previous 6 weeks) * Recent cardiac surgery (within the previous 8 weeks) * Unstable angina at the time of enrollment * History of embolism (cerebrovascular accident, transient ischemic attack, systemic embolism) in the previous 30 days * Previous cardiac ablation within the previous 30 days * EP ablation within the previous 6 weeks. * Life expectancy \<12 months per the physician opinion. * 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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites in 4 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Erasmus Medical Center
NOT_YET_RECRUITINGRotterdam, 3015 GD, Netherlands
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National Institute of Cardiology
NOT_YET_RECRUITINGWarsaw, 04-628, Poland
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Rigshospitalet, University of Copenhagen
RECRUITINGCopenhagen, Denmark
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Vilniaus universiteto ligoninė Santaros klinikos
RECRUITINGVilnius, Lithuania
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Other studies related to the condition(s) this trial covers.
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- Can a dual energy catheter tame dangerous heart rhythms?