MINDZ-- Minimally Invasive Approach Pilot Study
NCT: NCT07543406 · NOT_YET_RECRUITING
Brief Summary
This clinical investigation is a pilot, first-in-human (FIH) study designed to demonstrate proof of concept, safety, and functional performance of the MINDZ subdural electrode grid when used in relevant neurosurgical settings. The study will provide initial clinical evidence to support future conformity assessment and CE marking under the European Medical Device Regulation (MDR). The investigational device, MINDZ, developed by Neurosoft Bioelectronics, is a novel, soft and highly conformable subdural electrode grid designed for minimally invasive implantation through a burr hole. Its flexible structure is intended to improve conformity to the cortical surface, reduce dead space between the electrode and brain tissue, and potentially lower the risk of complications associated with craniotomy, while maintaining adequate cortical coverage for effective monitoring and mapping.
Frequently Asked Questions
What is MINDZ-- Minimally Invasive Approach Pilot Study?
MINDZ-- Minimally Invasive Approach Pilot Study is a clinical trial registered under NCT07543406. Current status: NOT_YET_RECRUITING.
What is the status of NCT07543406?
The current status of NCT07543406 (MINDZ-- Minimally Invasive Approach Pilot Study) is: NOT_YET_RECRUITING.
When did MINDZ-- Minimally Invasive Approach Pilot Study start?
MINDZ-- Minimally Invasive Approach Pilot Study started on 2026-05-01.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.