Graphene brain sensor tested in humans for first time
NCT ID NCT06368310
First seen Jun 24, 2026 · Last updated Jul 01, 2026 · Updated 4 times
Summary
This study tests a new graphene-based electrode array used during brain tumor surgery to map brain activity. Ten participants will have the device used alongside standard monitoring to check its safety and how well it records brain signals. If awake during surgery, they may do simple tasks to help decode brain signals. The goal is to see if this technology is safe and effective for future use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Graphene Cortical Interface (device)
- What this could lead to
- If successful, this could pave the way for safer, higher-quality brain mapping during surgery, potentially improving outcomes for brain tumor patients.
- What could go wrong
- This is a very early, small trial (10 people) focused on safety, not treatment. The device may not work as hoped, and risks include surgical complications or poor signal quality.
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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10 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Jun 2026
- 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: * Solitary supratentorial tumor radiologically consistent with glioma (intrinsic primary brain tumor) on standard diagnostic MRI; * Planned for surgery under awake conditions or under general anesthesia with intra-operative electrocorticography (ECoG); * English as first language for those subjects with tumors associated with language areas; * Karnofsky performance score \> 70 and World Health Organization (WHO) performance status score ≤ 1; * Willing and able to understand and provide informed consent for participating in the study. Exclusion Criteria: * Contraindications to magnetic resonance imaging (e.g., incompatible implanted devices); * Previous cranial surgery or radiotherapy; * Subjects expected to undergo craniotomy of less than 5 cm in maximum diameter (bone to bone) * Known extracranial malignant neoplasm; * Pregnant or lactating women; * Renal impairment sufficient to limit Gadolinium administration (EGFR \<60 ml/min) * For those subjects with tumors associated with language areas, any contraindication which could preclude them from performing the whole awake intra operative tasks at the discretion of the Investigator (e.g., language function not suitable for monitoring tasks)
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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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Manchester Centre for Clinical Neurosciences, Northern Care Alliance NHS Foundation Trust
Salford, Greater Manchester, M6 8HD, United Kingdom
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