Brain surgeons pinpoint the 'Arrival Time' region during awake operations
NCT ID NCT04128306
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study investigates which parts of the brain help us judge when a moving object will reach us, a skill used in daily life. Researchers test patients during awake brain surgery for tumor removal, using a simple task where they estimate when a disappearing object would have made contact. By stimulating different brain areas during the task, the team aims to create a map of the regions responsible for time-to-contact perception.
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 reveal which brain areas are essential for timing everyday actions like catching a ball or crossing a street.
- What could go wrong
- This is a small, early-stage mapping study, not a treatment trial. Results may not apply to all people or lead to direct clinical changes.
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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120 people
The number who actually took part.
- Started
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Sep 2019
- Finished
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Jan 2025
- 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 to 70 years
- 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.
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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: For the patients: * Brain tumor that does not affect the dominant hand motricity. The patient that have a tumor in an area targeted for a cortical stimulation will be automatically enrolled within the Pre-End group. * Who will agree with all terms and sign the experimental agreement * Correct or corrected vision, as allowed by the surgery constraints * With no known oculomotor abnormalities (list of exclusion in Annexe) * Affiliated to a social security system For the control group: * Who will agree with all terms and sign the experimental agreement * Correct or corrected vision * With no known oculomotor abnormalities. * Affiliated to a social security system Exclusion Criteria: For the patients: * Brain tumor located in the occipital area * Legally protected patient, or with unknown ability to sign the experimental agreement, as determined by the medical team. * Medical background of neurological diseases of the central nervous system, as Parkinson, Alzheimer, stroke * Pregnancy For the control group: * Legally protected patient, or with unknown ability to sign the experimental agreement, as determined by the medical team. * Medical background of neurological diseases of the central nervous system, as Parkinson, Alzheimer, stroke * 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
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University Hospital
Toulouse, 31000, France
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