Clinical Trial

StimRouter Registry Clinical Protocol

Study Description

StimRouter Registry Clinical Protocol

This Registry study will prospectively evaluate the long-term effectiveness, safety, and tolerability of the StimRouter Neuromodulation System, along with evaluating the technical performance of StimRouter, surgical outcomes, health-related quality of life, concomitant medical use, and subject's impression of improvement.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Device - StimRouter Neuromodulation System

An implantable neuromodulation device that treats chronic peripheral nerve pain.

Additional Information

Official Study Title

A Prospective, Open-label, Long-term, Multi-center, Registry to Assess the Safety and Efficacy of the Bioness StimRouter Neuromodulation System in Subjects With Chronic Pain of Peripheral Nerve Origin

Clinical Trial ID

NCT03913689

ParticipAid ID

aQW25d