New scan could reveal within days if brain tumor treatment is working
NCT ID NCT02902757
First seen Jun 26, 2026 · Last updated Jul 17, 2026 · Updated 2 times
Summary
This pilot study tested whether a type of PET/CT scan (FDG PET/CT) can detect very early changes in glioblastoma tumors after starting chemotherapy. Seven patients with high-grade glioma were scanned shortly after beginning therapy to see if changes in glucose uptake could predict later response. The goal was to find a way to quickly tell if treatment is working, potentially allowing doctors to adjust therapy sooner.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Fludeoxyglucose F-18 (FDG)
- What this could lead to
- If successful, this imaging method could help doctors quickly see if a glioblastoma treatment is working, allowing earlier adjustments.
- What could go wrong
- This was a very small pilot study with only 7 participants, so results may not apply to all patients. The technique is still experimental and not yet proven to improve 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.
- 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
-
7 people
The number who actually took part.
- Started
-
Aug 2015
- Finished
-
Jan 2025
- Lead sponsor
-
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
-
18 to 99 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients with histologically proven high grade glioma * Intention to start therapy Exclusion Criteria: * Severe psychiatric illness * Inability to give written consent * Breast feeding / pregnancy
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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
-
UCLA / Jonsson Comprehensive Cancer Center
Los Angeles, California, 90095, United States
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