Blood test could spare brain tumor patients from repeated surgeries
NCT ID NCT05133154
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study investigates whether a simple blood test can help diagnose and monitor low-grade gliomas, a type of slow-growing brain tumor. Researchers will collect blood samples from 50 patients undergoing brain surgery to look for circulating tumor cells and other markers. The goal is to find a non-invasive way to track tumor growth and detect changes without repeated biopsies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple blood test to help diagnose and monitor low-grade gliomas without repeated surgeries.
- What could go wrong
- This is an early exploratory study with only 50 participants. It may not find reliable blood markers, and results may not apply to all patients.
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 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2022
- Expected to finish
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Jul 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.
- 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: * Adult patient aged ≥ 18, no age limit * A signed informed consent obtained before any study specific procedures * Patient affiliated to a French social security system * Patient ability to understand experimental procedures * Patient able to speak, read and understand French Also for the "Low-grade glioma" group, the following inclusion criteria applies: \- Brain surgery for a suspected low-grade tumor, histologically confirmed on tumor sample Also for the "High-grade glioma" group, the following inclusion criteria applies: \- Brain surgery for a suspected high-grade glioma, histologically confirmed on tumor sample Also for the "Control group, the following inclusion criteria applies: \- Brain surgery for a non-tumor disease (cavernoma, arteriovenous malformation) Exclusion Criteria: * Legal incapacity or physical, psychological social or geographical status interfering with the patient's ability to sign the informed consent or to terminate the study * Pregnant and/or breastfeeding women (this will be checked in declarative way) * Patients with medical history of cancer other than the brain tumor, whatever the treatment received Also, for the "Low-grade glioma" group, the following exclusion criteria applies: * Previous chemotherapy or radiation therapy for the low-grade glioma (but previous surgery/ies is/are allowed) * No indication for chemotherapy for 6 month after surgery Also, for the "High-grade glioma" group, the following exclusion criteria applies: \- Previous chemotherapy or radiation therapy for the glioma Also, for the "control" group, the following exclusion criteria applies: \- Diagnosis or suspicion of primary or secondary brain tumor
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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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University Hospital, Montpellier
Montpellier, France
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Other studies related to the condition(s) this trial covers.
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