Brain tumor imaging study aims to find hidden cancer stem cells
NCT ID NCT01872221
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a special MRI technique can identify the most aggressive parts of a glioblastoma brain tumor. Researchers took tissue samples from different areas of the tumor during surgery and tested them for cancer stem cells. The goal was to see if MRI markers match the biology of the tumor, which could help guide future treatments. 21 patients took part in this early-stage research.
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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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21 people
The number who actually took part.
- Start date
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May 2013
- Finished
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Apr 2018
- 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.
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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: First part of the study (Surgery and Imagery): 1. Surgical indication for patients who present radiological criteria of glioblastoma. 2. Patient who are ≥18 years old 3. Patient must have performance status between 0 and 2 on the ECOG Performance Scale 4. Life expectancy ≥ 3 months 5. Patient affiliated to social security regimen 6. Patient has voluntarily agreed to participate by giving written informed consent for the first part of the study. Second part of the study (Treatment and Biology): 1. Histologically confirmed glioblastoma 2. Patient must have performance status between 0 and 2 on the ECOG Performance Scale or 3 only is due to motor deficit. 3. Life expectancy ≥ 3 months 4. Patient affiliated to social security regimen 5. Patient has voluntarily agreed to participate by giving written informed consent for the second part of the study. Exclusion Criteria: First part of the study (Surgery and Imagery): 1. Patients who are not allowed to perform an MRI 2. Spectroscopic exam whose results are not contributive 3. Pregnant or nursing patient, 4. Patients under law protection 5. Patient who presents conditions that would interfere with cooperation with the requirements of the trial. 6. Patient who presents medical, severe or chronic biological or psychiatric conditions not allowing his enrolment in the study, according to the investigator's opinion Second part of the study (Treatment and Biology): 1.Biological material received in the lab more than 48 hours after surgery.
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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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CHU Rangueil
Toulouse, 31000, France
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Institut Claudius REGAUD
Toulouse, 31052, France
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Other studies related to the condition(s) this trial covers.
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