New heart imaging tool tested in first human study
NCT ID NCT07353710
First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 4 times
Summary
This study will test a new imaging system called CHORUS IDx in 200 people scheduled for a heart ablation procedure. The system takes pictures inside the heart to help doctors see better during the procedure. The main goal is to check if the device is safe and to collect images that will be used to improve the software.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help improve imaging software for guiding heart procedures, potentially making them safer and more effective.
- What could go wrong
- This is a very early, first-in-human study focused on data collection, not treatment. The device may not work as expected, and there is a risk of procedure-related side effects.
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 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2026
- Expected to finish
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Dec 2027
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: 1. Subjects who are able and willing to provide written informed consent prior to any study procedure. 2. Subjects who are planned for an ablation procedure for any atrial arrhythmia using any commercially available Boston Scientific Ablation System, per physician's judgement and hospitals' standard practice. 3. Subjects who are willing and able to participate in all testing and assessments associated with this clinical study at an approved clinical investigation center. 4. Subjects whose age is 18 years or above, or who are of legal age to give informed consent specific to state and national law. Exclusion Criteria: 1. Any of the following cardiac implanted devices * Any prosthetic mitral or tricuspid heart valve, such as ring, repairs or clips * Atrial septal defect (ASD) occluders including interatrial baffle, closure device, patch, or patent foramen ovale or ASD occluder 2. Subjects with contraindications related to the use of the CHORUS IDx™ System: * Subjects with inadequate vascular access * Subjects with active systemic infection * Subjects with presence of a known intracardiac thrombus in the chamber of use 3. Women who are confirmed to be pregnant or lactating at the time of the Index Procedure 4. Presence of other medical conditions, that, in the investigator's opinion, could limit the subject's ability to participate in the study 5. Subjects who are currently enrolled in another investigational study or registry that would directly interfere with the current study, except when the subject is participating in a mandatory governmental registry, or a purely observational registry with no associated treatments; each instance must be brought to the attention of the Sponsor to determine eligibility
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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
8 sites in 8 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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Auckland City Hospital
NOT_YET_RECRUITINGAuckland, New Zealand
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Hygeia Hospital
NOT_YET_RECRUITINGAthens, Greece
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IKEM - Institut klinicke a experimentalni mediciny
NOT_YET_RECRUITINGPrague, Czechia
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Institut Jantung Negara
NOT_YET_RECRUITINGKuala Lumpur, Malaysia
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Klinicki Bolnicki Centar Split
RECRUITINGSplit, Croatia
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Lingard Private Hospital
NOT_YET_RECRUITINGMerewether, Australia
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National Heart Center Singapore
RECRUITINGSingapore, Singapore
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Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego
NOT_YET_RECRUITINGWarsaw, Poland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a common heart drug stop rhythm problems after a Stroke-Related heart repair?
- Can targeted electrical pulses quiet an erratic heartbeat?
- AI maps the way to better heart ablation?
- New Dual-Action heart procedure could tame stubborn AFib
- Heart ablation after pouch closure: new registry data collected
- New heart procedure aims to tame atrial fibrillation without drugs