New scan may sharpen radiation targeting for brain cancer patients
NCT ID NCT02104310
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether adding a special PET scan (18F-DOPA) to the standard MRI can help doctors better plan radiation treatment for people with certain brain tumors (malignant glioma). The PET scan may show tumor tissue more clearly than MRI alone. About 25 participants aged 7 and older with grade II or III glioma will be enrolled. The goal is to compare treatment areas defined by MRI versus MRI plus the PET scan.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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25 people
The number who actually took part.
- Started
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Apr 2014
- Expected to finish
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Mar 2031
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
Newly diagnosed or recurrent WHO Grade II and Grade III Glioma patients.
- Ages
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7 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: * Age ≥7 years. * Biopsy confirmed newly diagnosed or recurrent WHO Grade II or Grade III malignant glioma. * CT simulation, 18F-DOPA PET imaging, and standard of care pre-radiotherapy MRI scans to be performed at Mayo Clinic Rochester. * Willing to sign release of information for any follow-up records. * Provide informed written consent. Exclusion Criteria: * Patients diagnosed with WHO grade IV malignant glioma. * Patients previously treated with radiation therapy. * Unable to undergo MRI scans with contrast (e.g. cardiac pacemaker, defibrillator, kidney failure). * Unable to undergo an 18F-DOPA PET scan (e.g. Parkinson's Disease, taking anti-dopaminergic, or dopamine agonist medication or less than 6 half-lives from discontinuance of dopamine agonists) * Pregnant women * Nursing women * Men or women of childbearing potential who are unwilling to employ adequate contraception
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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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Mayo Clinic
Rochester, Minnesota, 55905, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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