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NCT03913689 · ClinicalTrials.gov registry record
StimRouter Registry Clinical Protocol
A clinical trial of Chronic Pain and Peripheral Neuropathy, sponsored by Bioness.
- Completed
- Registry status
- 62
- Enrollment target
- 9
- Study locations
NCT03913689 is a study of Chronic Pain and Peripheral Neuropathy that has completed, run by Bioness. The registered enrollment target is 62 participants, below the 772-participant average among 301 other Chronic Pain trials with a reported enrollment target (92% lower). The trial reports 9 study locations across 7 states.
The verdict
NCT03913689, a study of Chronic Pain and Peripheral Neuropathy, has completed, sponsored by Bioness.
- COMPLETED
- Registry status
- 62 participants
- Enrollment target
- 9
- Study locations
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.
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 62 participants |
| Start Date | 2019-06-26 |
| Est. Completion | 2024-06-30 |
Interested in This Trial?
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, categorized as an unspecified phase. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 772-participant average among 301 other Chronic Pain trials with a reported enrollment target (92% lower). The listed sponsor is Bioness, which has 6 total studies on file at ClinicalTrials.gov.
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.
NCT03913689 reports 9 study locations spanning 7 distinct geographic areas - top geographies include California, Connecticut, District of Columbia.
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.
What interventions are being tested in trial NCT03913689?
The interventions under investigation include: StimRouter Neuromodulation System (DEVICE).
Who is sponsoring clinical trial NCT03913689?
This trial is sponsored by Bioness, which has 6 total clinical trials registered on ClinicalTrials.gov.
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.
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