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Age: 18Years +
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ID04733599

High Frequency Spinal Cord Stimulation for Neuropathic Pain Following Brachial Plexus Avulsion Injury a Prospective Observational Cohort Study

Led by Mayo Clinic · Updated on 2026-03-02

20

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to observe how high frequency spinal cord stimulation therapy affects pain intensity in adults with serious brachial plexus avulsion injury causing chronic neuropathic pain in the upper limb. The study focuses on adults over 18 years old who are candidates for this specific neurostimulation treatment and seeks to understand its impact over time. Participants will undergo implantation of a high frequency HF10 spinal cord stimulation device to manage their chronic upper limb neuropathic pain. The study is observational, following patients who receive this therapy without comparing to a placebo or other treatment. Researchers will monitor changes in pain and related symptoms over multiple scheduled time points. Throughout the study, participants will be evaluated at baseline and then at 1, 3, 6, 12, 18, 24, and 36 months after implantation. Assessments include neuropathic pain levels, pain intensity, pain interference, and quality of life questionnaires. Additional measures cover disability, mood, pain anxiety, and sensory function in the affected limb. This long-term follow-up helps researchers understand the therapys effects and patient experiences over three years.

CONDITIONS

Brief Title

Neurostimulation for Treatment of Chronic Upper Limb Pain After Brachial Plexus Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years old
  • Neuropathic pain of the upper limb lasting 3 months or more following brachial plexus avulsion injury
  • Planned implantation of high-frequency spinal cord stimulation for chronic neuropathic pain due to brachial plexus avulsion injury
Not Eligible

You will not qualify if you...

  • Non-neuropathic pain as indicated by DN4 score less than 4
  • Pregnant or planning to become pregnant during the study
  • Active substance use disorder
  • Active tobacco use
  • Use of moderate or high dose opioid medication (over 100 mg oral morphine equivalents daily)
  • Active, untreated major psychiatric disorder interfering with participation
  • Involvement in active litigation related to injury
  • No prior conservative medical management for at least 3 months, including physical or occupational therapy and neuropathic pain medication trial

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