common.study.topics.clinical

StimRouter Registry Clinical Protocol

common.study.values.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.

common.study.values.location

participant.ui.study.affiliations-map.online-study.header-virtual

participant.ui.study.affiliations-map.online-study.text

participant.ui.study.affiliations-map.legend.locations participant.ui.study.affiliations-map.legend.selected

common.study.values.methods

No pharmaceutical medication involved common.study.methods.has-drugs-no
Patients and healthy individuals accepted common.study.methods.is-healthy-no

Device - StimRouter Neuromodulation System

An implantable neuromodulation device that treats chronic peripheral nerve pain.

participant.views.study.view.additional

participant.views.study.view.scientific-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

common.study.values.clinical-trial-id

NCT03913689

participant.views.study.view.id

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