New CT scanner aims to cut unnecessary heart procedures
NCT ID NCT07831304
First seen Sep 21, 2026 ยท Last updated Sep 21, 2026
Summary
Researchers compare two types of CT scanners for imaging heart arteries in people with suspected chronic coronary syndrome. One scanner uses standard energy-integrating detectors, while the other uses newer photon-counting detectors that may produce clearer pictures with fewer false alarms. The trial tracks how often each scan correctly identifies narrowed arteries, along with costs and follow-up care over two years. About 630 adults who need a coronary CT angiogram take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- photon-counting detector CT (PCD-CT) versus energy-integrating detector CT (EID-CT) for coronary CT angiography
- What this could lead to
- If photon-counting CT proves more accurate, it could reduce unnecessary invasive heart procedures and lower healthcare costs for people with suspected coronary artery disease.
- What could go wrong
- The trial may show no meaningful difference between the two scanners, or the newer technology may not be widely available or affordable. Results from this single healthcare system may not apply elsewhere.
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
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About 630 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2026
- Expected to finish
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Sep 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
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: * clinical indication to perform CCTA for CAD assessment according to 2024 ESC Guidelines Exclusion Criteria: * Refusal to participate in the study * Age \<18 years old * Severe reduction in eGFR (\<30 mL/min)
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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.
Contacts and locations
Locations
-
Advanced Imaging for Personalized Medicine/Radiologia DiMer
Milan, Milano, 20132, Italy
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