Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07465796

A First-in-Human Study of the CIPHER System During Brain Surgery for Newly Diagnosed Glioma

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Coherence Neuro Australia Pty Limited · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The goal of this clinical trial is to collect data on the use of the CIPHER System when used by a surgeon during brain tumor removal. The main questions it aims to answer are: * To evaluate the safety of the CIPHER System when used during brain tumor surgery (Primary) * To evaluate the function of the electrodes under recording and stimulating conditions during surgery (Secondary) Participants will undergo standard-of-care surgery to remove their tumor. Just before the tumor is removed, the CIPHER System will be tested on the main tumor and the surrounding margin areas. Participants will be monitored during standard hospital visits occurring during the recovery period after surgery as well as two- and six-weeks after surgery.

Detailed description

Brain tumor resection surgery involves a balance between removing tumor and preserving healthy tissue. Current standard-of-care mapping tools use limited electrode configurations on rigid substrates to stimulate and record brain activity for identifying functional brain areas to avoid. A more flexible and high electrode-count tool to map the tumor characteristics based on spontaneous neural activity could strengthen surgical outcomes. Emerging evidence also demonstrates that brain tumors, such as gliomas, are not biologically isolated but instead integrate functionally into neural circuits. Electrical stimulation-based strategies could provide novel treatment modalities that target the neural-tumour interactions and improve patient outcomes. This clinical investigation is a First-in-Human exploratory study of the CIPHER System, including a novel highly flexible, electrode-dense thin-film cortical probe developed for neurophysiological mapping and stimulation during brain tumour resection surgery. The study is designed to evaluate the safety, basic performance, and handling characteristics of the CIPHER System during short-duration intraoperative use.

Conditions

Interventions

TypeNameDescription
DEVICEElectrocorticography for neural recordingElectrocorticography probe placed on the brain surface for neural recording
DEVICEElectrocorticography for neural recording and electrical stimulationElectrocorticography probe placed on the brain surface for neural recording and electrical stimulation

Timeline

Start date
2026-03-01
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2026-03-12
Last updated
2026-03-12

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT07465796. Inclusion in this directory is not an endorsement.