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RECRUITING
NCT07546253

Post-Market Real-World Evidence Registry for the NeuroOne OneRF® Ablation System for Epilepsy

Sponsor: NeuroOne Medical Technologies Corporation

View on ClinicalTrials.gov

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

OTHER

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