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COMPLETED

StimRouter Registry Clinical Protocol

NCT03913689 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE StimRouter Neuromodulation System

Study Locations (9)

California

  • University of California San Diego — La Jolla
  • California Orthopedics & Spine — Larkspur
  • Stanford University — Redwood City

Connecticut

  • Stamford Hospital — Stamford

District of Columbia

  • International Spine,Pain and Performance Center — Washington D.C.

Louisiana

  • Warner Orthopedics — Baton Rouge

Pennsylvania

  • Albert Einstein/Moss Rehab — Elkins Park

Virginia

  • Valley Sports and Spine Clinic — Blacksburg

Wisconsin

  • Advocate Aurora Health — Oshkosh

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2019-06-26
Est. Completion 2024-06-30

Sponsor

Bioness

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03913689

The ClinicalTrials.gov registry entry for NCT03913689 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bioness, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 7 conditions, with Chronic Pain appearing as the primary indexed condition, and to 1 intervention — of which StimRouter Neuromodulation System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03913689 reports 9 study locations spanning 7 distinct geographic areas — top geographies include California, Connecticut, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03913689 about?

NCT03913689 is a clinical study titled "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 imp...

What is the current status of trial NCT03913689?

This trial is currently completed. The enrollment target is 62 participants. The study started on 2019-06-26. Estimated completion is 2024-06-30.

What conditions does trial NCT03913689 study?

This clinical trial studies the following conditions: Chronic Pain, Peripheral Neuropathy, Nervous System Diseases, Peripheral Nerve Injuries, Peripheral Nervous System Diseases. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03913689?

The interventions under investigation include: StimRouter Neuromodulation System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03913689?

This trial is sponsored by Bioness, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03913689 being conducted?

This trial has 9 study locations across California, Connecticut, District of Columbia, Louisiana, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial