AI spots hidden brain aneurysms in routine scans
NCT ID NCT07123818
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether an AI program can find unruptured brain aneurysms on standard CT scans that people already get for other reasons. Ten adults with risk factors (like high blood pressure or being over 40) will have their scans checked by AI and then by a radiologist. The goal is to see if AI can help catch aneurysms early without extra cost or radiation.
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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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10 people
The number who actually took part.
- Started
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Oct 2025
- Expected to finish
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Dec 2030
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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Accepted
You do not need to have the condition being studied to take part.
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: * the subject of the NECT scan must be an adult patient (Age ≥ 18 years old); * the NECT scan must be a NECT scan from the brain; * the NECT scan must contain the entire brain * the patient should have at least one of the following risk factors for developing a brain aneurysm * patient is female * patient has a family history of brain aneurysms * patient is 40 years or older * patient has or is treated for a high blood pressure * patient actively smokes cigarettes at time of inclusion * a first informed consent form must be signed before brain NECT scans can be transferred to Robovision * a second signed written informed consent must be obtained before follow-up data will be gathered, if applicable. Exclusion Criteria: \- There are no specific exclusion criteria.
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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
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AZ Groeninge
Kortrijk, 8500, Belgium
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UZ Brussel
Brussels, 1090, Belgium
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Ziekenhuis Oost-Limburg - campus Maas en Kempen
Maaseik, 3680, Belgium
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Ziekenhuis Oost-Limburg - campus Sint-Jan
Genk, 3600, Belgium
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Other studies related to the condition(s) this trial covers.
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