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Post-Market Real-World Evidence Registry for the NeuroOne OneRF® Ablation System for Epilepsy
Sponsor: NeuroOne Medical Technologies Corporation
Summary
This is a multi-site registry study that aims to collect real-world clinical outcomes and device performance of the OneRF Ablation System. The study focuses on patients with refractory epilepsy who undergo, or are being considered for, sEEG-guided RF ablation using the OneRF Ablation System, as part of routine seizure diagnosis and treatment.
Official title: OneRF® Ablation System Post-Market Real-World Evidence Registry
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2026-09-18
Completion Date
2028-07
Last Updated
2026-10-16
Healthy Volunteers
No
Interventions
Participants are not assigned an intervention as part of the study.
For observational studies, participants are not assigned an intervention as part of the study.
Locations (3)
Nicklaus Children's Hospital
Miami, Florida, United States
Cooperman Barnabas Medical Center - 94 Old Short Hills Rd
Livingston, New Jersey, United States
Robert Wood Johnson University Hospital - 1 Robert Wood Johnson Pl
New Brunswick, New Jersey, United States