New PET scan method aims to outsmart brain tumor comebacks
NCT ID NCT07599917
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at 69 past brain scans using a special tracer called [18F]FET to see if it can more accurately tell the difference between a returning tumor and changes caused by previous treatment. Researchers will analyze both still and time-lapse images to find better ways to diagnose and classify brain tumors. The goal is to improve how doctors use this type of PET scan in everyday care.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 69 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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.
Who is studied
Adult patients (≥18 years) who underwent clinically indicated \[18F\]FET PET/CT or PET/MR brain scans for evaluation of primary or metastatic brain tumors, including diagnosis, grading, treatment response assessment, or suspected recurrence.
- 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: * Patients who underwent a brain PET/CT or PET/MRI scan with \[18F\]FET for clinical reasons during the study period. * Age ≥ 18 years. * Indication for the scan related to diagnosis, grading, assessment of treatment response or suspected recurrence of any brain tumour (primary or metastatic). * Availability of the corresponding static and dynamic images. * Signed informed consent. Exclusion Criteria: * . Pregnancy or breastfeeding
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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 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.
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Other studies related to the condition(s) this trial covers.
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