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Magnetic heart fix: new device targets dangerous rhythms

NCT ID NCT06019845

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 150 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2024

Expected to finish

Dec 2028

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

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.

Arrhythmias, Cardiac atrial fibrillation atrial flutter cardiac rhythm disease Tachycardia, Supraventricular Ventricular Premature Complexes ventricular tachycardia

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.

  1. The places running it

    4 sites in 4 countries. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Erasmus Medical Center

    NOT_YET_RECRUITING

    Rotterdam, 3015 GD, Netherlands

  • National Institute of Cardiology

    NOT_YET_RECRUITING

    Warsaw, 04-628, Poland

  • Rigshospitalet, University of Copenhagen

    RECRUITING

    Copenhagen, Denmark

  • Vilniaus universiteto ligoninė Santaros klinikos

    RECRUITING

    Vilnius, Lithuania

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