Clinical Trial

Evaluation of New Flexible High-density Intra-operative ECoG Electrodes for Epilepsy Surgery. ( EpiGrid )

Study acronym: EpiGrid
Recruiting
View on ClinicalTrials.gov →
Summary
The objective of this prospective interventional monocentric clinical investigation is to evaluate the feasibility and performance of the flexible high-density SOFT ECoG electrode grids, manufactured by Neurosoft Bioelectronics SA (test device; TD), in comparison to regular high-density electrode grids (ADTech, CE-marked) (control device; CD) routinely used at the investigation site during epilepsy surgery. Subjects will undergo ≥ 2 additional intracranial recordings pre- and post-resection with the TD next to the standard recordings with the CD during ECoG-tailored epilepsy surgery.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-01-03; most recent amendment 2025-12-09.
Status change: Not Yet Recruiting → Recruiting 2025-01-13
Trial Details
NCT Number NCT06205160
Lead Sponsor Neurosoft Bioelectronics SA
Collaborators: UMC Utrecht, European Research Council
Conditions Focal Epilepsy, Intraoperative Monitoring
Enrollment 12 participants
Start Date 2025-01-01
Primary Completion 2027-03 (estimated)
Study Completion 2027-03 (estimated)
Updated on ClinicalTrials.gov 2025-12-10