Can AI make CT scans sharper and more reliable?
NCT ID NCT07767201
First seen Aug 17, 2026 · Last updated Aug 18, 2026 · Updated 1 time
Summary
This trial evaluates whether an AI-based image reconstruction algorithm, called Precise Image, produces CT scan images that are as good as or better than the current standard method. The study involves adults who have had CT scans using specific Philips systems. The goal is to see if the AI can provide images that are diagnostically acceptable for doctors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Precise Image, an AI-based image reconstruction algorithm for CT scans
- What this could lead to
- If successful, this could support the use of AI-based image reconstruction in routine CT scans, potentially improving image quality and diagnostic accuracy.
- What could go wrong
- This is an early-stage evaluation, and the AI may not perform as well as standard methods in all cases. The trial focuses on image quality, not direct patient outcomes.
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.
- Participants
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About 192 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Mar 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.
Who is studied
Subjects that are adults over the age of 22 years and scanned by CT Rembra RT, CT Areta RT or CT Rembra.
- Ages
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23 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: * Subjects scanned by CT Rembra RT, CT Areta RT or CT Rembra according to the department standard of care clinical protocols. * Subjects age \> twenty-two (22) years Exclusion Criteria: * Scans that the site radiologists/medical physicists have deemed as non-diagnostic image quality in the standard practice (e.g. patient movement) * Scans that are not completed due to technical difficulties
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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 official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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