Peripheral Neuropathy Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have had a traumatic spinal cord injury at or above the T1 level (roughly the upper back or neck), either within the last 6 months (and considered medically stable) or more than 6 months ago, with any level of impairment severity.
- People who have had a peripheral nerve injury (with or without a spinal cord injury) and are either before or after surgery to transfer nerves in the arm or hand — either within 6 months of that surgery (considered medically stable and appropriate to participate by their neurosurgeon) or 6 or more months after surgery.
- People who show at least some response in an arm or hand muscle on the affected side when electrical stimulation is applied to that muscle, confirmed at a baseline assessment.
- People who show at least some detectable voluntary muscle activity in at least one arm or hand muscle on the affected side, confirmed by electrical muscle testing at a baseline assessment.
- For one part of the study only: people who are able to commit to treatment and assessment sessions over a period of up to 4 months.
Who may not be able to join:
- People who have a traumatic brain injury, stroke, multiple sclerosis, or another condition that could affect how the nerves and muscles work.
- People with severe muscle stiffness or spasms that could prevent them from taking part in the study, as assessed by the investigator.
- People with significant difficulties in thinking, memory, or mental health — including dementia, major depression, or other serious medical conditions affecting cognition.
- People for whom electrical skin stimulation would not be safe — for example, those with broken or damaged skin where the electrodes would be placed, blood clots, or a skin disease in the relevant area.
- People with poorly controlled autonomic dysreflexia (a condition involving sudden high blood pressure) that could be triggered by electrical stimulation.
- People with an unhealed bone fracture, joint stiffening, or pressure sore in the arm or hand.
- People who have an implanted nerve stimulation device, such as a deep brain stimulator or vagal nerve stimulator.
- People who have a cardiac pacemaker or electrical lines inside the heart.
- People who require other treatments or care that could interfere with taking part in the study.
- People who are currently taking experimental drugs or other treatments known to affect nerve and muscle function.
- People with substance use disorders, including alcohol or drug dependency.
- People who are pregnant, breastfeeding, or planning to become pregnant during the study period.
- People who the investigators consider unsuitable or unsafe for the study for any other reason.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Matija Milosevic, PhD, University of Miami
Phone: (305) 243-9301
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Nine Hole Peg Test; Surface EMG; Graded-Redefined Assessment of Strength, Sensibility, and Prehension (GRASSP) Prehension Performance (GR-PP); Manual Muscle Test (MMT) with FES
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.