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NCT03093935 · ClinicalTrials.gov registry record · NA

StimRouter™ for Pain Management in Post-stroke Shoulder Pain

A NA study, sponsored by Bioness.

Terminated
Registry status
NA
Development phase
6
Enrollment target

NCT03093935: Clinical Trial NA study, sponsored by Bioness.

NCT03093935 is a NA study that was terminated before completion, run by Bioness. The registered enrollment target is 6 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03093935, a NA study, was terminated before completion, sponsored by Bioness.

TERMINATED
Registry status
NA
Development phase
6 participants
Enrollment target

Study Summary

StimRouter Neuromodulation System includes an implanted lead which provides peripheral nerve stimulation for chronic pain. Post-stroke shoulder pain patients will be the focus of this study. After meeting inclusion/exclusion criteria, approximately 50 enrolled patients will participate in the study through 6 months of follow-up. Various measures will be used to assess patient response to use of the device.

Primary Outcome

The Brief Pain Inventory (BPI) form is a standard pain assessment tool based on a 0 to 10 scale. The Average Pain at Rest (BPI question number 5) score will be assessed at Baseline and approximately 3 months after programming (therapy start) to determine if there is a significant reduction in average pain with the addition of StimRouter TM treatment to standard of care.

Interventions

  • DEVICE StimRouter Neuromodulation System

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2018-07-01
Est. Completion 2020-11-20
Phase NA
Bioness

6 total trials

Why NCT03093935 stopped before completion

NCT03093935 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 1 intervention - of which StimRouter Neuromodulation System is the first listed.

NCT03093935 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03093935 about?

NCT03093935 is a clinical study titled "StimRouter™ for Pain Management in Post-stroke Shoulder Pain". StimRouter Neuromodulation System includes an implanted lead which provides peripheral nerve stimulation for chronic pain. Post-stroke shoulder pain patients will be the focus of this study. After meeting inclusion/exclusion criteria, approximately 50 enrolled patients will participate in the study ...

What is the current status of trial NCT03093935?

This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2018-07-01. Estimated completion is 2020-11-20.

What interventions are being tested in trial NCT03093935?

The interventions under investigation include: StimRouter Neuromodulation System (DEVICE).

Who is sponsoring clinical trial NCT03093935?

This trial is sponsored by Bioness, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03093935's enrollment target sits among peer trials

6 1983rd of 2000 higher than 13 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03093935, the US trial registry maintained by the National Library of Medicine. NCT03093935 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.