Starving brain tumors of blood before surgery
NCT ID NCT07823985
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Some brain tumors, including meningiomas, hemangioblastomas, and certain metastases, have a rich blood supply that makes surgical removal difficult and risky. This study tests whether blocking the tumor's feeding blood vessels with a catheter procedure before surgery reduces bleeding and helps surgeons remove the tumor more safely. Participants undergo imaging, the embolization procedure, and then microsurgical tumor removal within one to three days. Researchers track how much of the tumor's blood supply is cut off, how much blood is lost during surgery, and any complications.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Preoperative endovascular embolization, a catheter procedure that blocks the tumor's feeding blood vessels using particles, Onyx, or microcoils
- What this could lead to
- If it works, doctors could use this catheter technique to make surgery safer and more complete for people with highly vascular brain tumors.
- What could go wrong
- This is a small, single-center study with no comparison group, so results may not apply broadly. Embolization carries risks of stroke, bleeding, or vessel damage, and not every tumor can be safely reached.
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 55 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
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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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: * Diagnosis of a hypervascular brain tumor (e.g., meningioma, hemangioblastoma, or hypervascular metastasis) confirmed by contrast-enhanced MRI or CT * Scheduled for preoperative endovascular embolization followed by microsurgical resection Exclusion Criteria: * Severe, uncorrected coagulopathy * Severe allergy to iodinated contrast media * Severe renal insufficiency (estimated glomerular filtration rate \[eGFR\] \< 30 mL/min/1.73 m²) * Absence of safe arterial access * Absence of identifiable tumor-feeding vessels suitable for selective microcatheterization
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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
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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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