RecruitingNot applicableEN originalGlioma (brain cancer)Metastatic / advanced

Pilot IntraOperative Neuronal Electrophysiology in Tumor rElatEd suRgery

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

INTRODUCTION AND RATIONALE Aggressive brain tumors like glioma have the ability to infiltrate the surrounding healthy brain tissue, disrupting normal neuronal activities and leading to impaired motor and cognitive functions, as well as causing epilepsy. This malignant brain tumor is considered one of the most challenging cancers to treat, with a median survival of 12 to 15 months. Recent findings on direct neuron-tumor interactions indicate that abnormal brain activity in the regions surrounding brain tumours may contribute to develop epilepsy and accelerating tumor growth. Tumors tend to 'fuel' themselves with neurotransmitters released during its 'daily' neuronal firing. Hyperactive neurons in the peritumoral cortex can form excitatory electrochemical synapses with surrounding tumor cells, creating direct communication pathways within the peritumoral microenvironment, which aids in the progression and proliferation of tumor cells via direct and paracrine signalling pathways. However, the specific features of this abnormal brain activity in the peritumoral cortex have not been fully clarified and information on the pathological changes of neuronal activity in glioma patients is largely lacking. To advance more effective treatment strategies, it is crucial to better understand the complex interactions between the tumor and the brain. This is especially important for our group of patients of which many perceive diminished quality of life because of epilepsy, cognitive functioning and language problems after tumor surgery. Furthermore, we lack thorough understanding of what tumor resection does to the original hyperactive peritumoral cortex and if resecting this is beneficial for improving postoperative outcome both for epilepsy as well as regarding survival. Therefore, identifying the hyperactive peritumoral cortex and directly addressing its impacts on the brain function and long-term surgical outcome could be a promising novel therapeutic strategy for treating glioma patients. STUDY AIM Our measurement focuses on capturing neuronal activity at single-neuron resolution in the peritumoral cortex of glioma patients using cortical depth electrodes. It is well-established that gliomas can remodel the surrounding brain tissue, leading to abnormal neuronal hyperactivity, which contributes to tumor progression and epilepsy. However, the specific neuronal patterns and underlying mechanisms of these changes are not yet fully understood. Our study will aim to collect detailed single-neuron recordings in this context, enabling us to map the precise neurophysiological disruptions caused by gliomas. On the long term, our research could lay the groundwork in identifying novel therapeutic approaches by providing critical in-sights into how gliomas alter brain function.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Wiek powyżej 18 lat
  • •Potwierdzony radiologicznie guz mózgu (glejak lub przerzuty)
  • •Kwalifikacja do operacyjnego usunięcia guza lub biopsji
  • •Pisemna zgoda na uczestnictwo w badaniu
  • •Możliwość monitorowania mózgu podczas operacji

✗ Disqualifies

  • •Historia poważnych chorób psychiatrycznych (schizofrenia, zaburzenie dwubiegunowe, oporna depresja)
  • •Poprzednia operacja mózgu lub radioterapia
  • •Rozrusznik serca lub inne urządzenia elektroniczne wszczepione w ciele
  • •Brak możliwości wyrazenia świadomej zgody

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
October 5, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Erasmus MC, Department of Neurosurgery

Rotterdam, Netherlands

Trial contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 10/6/2026.

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