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Oxygen-Enhanced MRI could sharpen radiotherapy for deadly brain cancers
NCT ID NCT07670455
First seen Jun 27, 2026 · Last updated Jul 01, 2026 · Updated 2 times
Summary
This study tests whether oxygen-enhanced MRI (OE-MRI) can identify low-oxygen (hypoxic) regions in high-grade gliomas, the most common and aggressive adult brain cancers. Twenty-five patients will undergo OE-MRI scans before, during, and after standard radiotherapy. Researchers will then use computer models to see if targeting those hypoxic areas with higher radiation doses could improve tumor control. The study does not change actual treatment—it is purely imaging and planning.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Oxygen-enhanced MRI (OE-MRI)
- What this could lead to
- If successful, this imaging technique could help doctors target radiotherapy more precisely to low-oxygen tumor areas, potentially improving treatment for aggressive brain cancers.
- What could go wrong
- This is a small, early-stage imaging study (25 participants) that only models higher radiation doses—it does not test actual treatment changes. The technique may not reliably detect hypoxia or 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
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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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About 25 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2028
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: * ≥18yrs. * Participants able to communicate with staff and safely comply with the study procedures. * Participants to provide informed written consent. Exclusion Criteria: * Participants with any MRI contraindications including inability to lie flat in MRI scanner, claustrophobia and no foreign bodies, medical devices or other items which are considered an MRI contraindication. * Geographically remote patients unable to agree to imaging schedule. * Participants with illness or condition which means they cannot understand the requirements of the study. * Participants with cardiac or pulmonary disease that are unable to tolerate the flow of oxygen delivered via a mask. * Participants who have previously been treated with bleomycin (a chemotherapy used to treat some cancers including Hodgkin lymphoma and germ cell tumours). * Participants with contraindications to gadolinium-based contrast agent
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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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