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

Recruitingn/aAges any - anyAllNeuroOne Medical Technologies Corporation
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In plain words

What the trial is, and whether it could suit you

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.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. Patients diagnosed with drug resistant epilepsy (DRE) 2. Patients who have received or will receive EVO® sEEG-RF implants 3. Patients who have undergone or may undergo an RF ablation procedure using the OneRF Ablation System. 4. Patient, or legal guardian, understands study procedures and voluntarily signs informed consent in accordance with institutional policies. In the event that the patient is under the age of 18, the patient may also be required (per IRB) to sign an assent affirming their agreement to participate. Exclusion Criteria: 1\. Any condition that, in the judgement of the clinician, would make the participant inappropriate for registry participation
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What it tests

  • Participants are not assigned an intervention as part of the study.
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Where

3 sites
Nicklaus Children's Hospital
Miami, United States
Cooperman Barnabas Medical Center - 94 Old Short Hills Rd
Livingston, United States
Robert Wood Johnson University Hospital - 1 Robert Wood Johnson Pl
New Brunswick, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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