TerminatedNot Applicable

AcQMap® Global Registry of Procedural and Long-term Clinical Outcomes (AcQMap Registry)

Stopped: Sponsor no longer performing clinical studies. Will be only a manufacturing facility

France, Germany, Netherlands479 participantsStarted 2019-06-13

Plain-language summary

AcQMap Registry is an observational study

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male or female 18 years of age or older. * Currently scheduled for an ablation of an arrhythmia utilizing the diagnostic AcQMap System. * Willingness, ability and commitment to participate in baseline and follow-up evaluations for the full length of the study. * Willing and able to give written informed consent. Exclusion Criteria: * In the opinion of the Investigator, any known contraindications to an ablation procedure. * Current enrollment in any study protocol sponsored by Acutus Medical. * 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.).

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Procedural Ablation Outcomes

Timeframe: 12 hours

Trial details

NCT IDNCT03893331

SponsorAcutus Medical

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2023-11-08

View on ClinicalTrials.gov More Ablation of Arrhythmia's trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.