Spinal stimulation may reawaken paralyzed arms — a trial puts it to the test
NCT ID NCT07722429
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This trial investigates whether a surgically implanted device that delivers personalized electrical stimulation to the spinal cord can improve upper limb function in people with spinal cord injury. Twenty participants with injuries at or above the T4 level will receive the implant along with a structured rehabilitation program. The study measures changes in independence, dexterity, and neurological function to see if this approach can help restore movement and daily living skills.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a surgically implanted device that delivers epidural electrical stimulation to the cervical spinal cord, combined with physical rehabilitation
- What this could lead to
- If it works, this approach could offer a way to restore hand and arm function in people with spinal cord injury, improving independence in daily life.
- What could go wrong
- This is a small early-stage trial with only 20 participants, so results may not apply to everyone. The surgical implantation carries risks such as infection or device complications, and not all participants may see meaningful improvement.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 20 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age between 18 and 70 years. * Duration since spinal cord injury ranging from 1 to 10 years. * Spinal cord injury level at or above T4. * MRI and/or CT imaging confirms adequate spinal cord decompression and spinal stability. * Stable vital signs and no dependence on mechanical ventilation. * Stable neurological and psychological status, with no history of neurological deterioration within the past 6 months (e.g., acute worsening of motor or sensory function, new-onset seizures, acute changes in muscle tone, or other neurological symptoms). Participants must be conscious, able to understand, and comply with study instructions. Clinical neurological examinations and imaging findings (MRI or CT) should demonstrate no new abnormalities. * Willingness to participate in and comply with rehabilitation programs. * Participants who have completed spinal cord electrical stimulation implantation surgery and/or are currently undergoing conventional rehabilitation therapy. Exclusion Criteria: * Patients with untreated fractures of the upper extremities. * Patients with severe skin lesions or wounds that interfere with EMG electrode placement or the surgical sites for electrical stimulation implantation (e.g., chest/back, upper extremities, posterior cervical region, or subclavicular area). * Patients with a history of other neurological diseases. * Patients with known allergy or hypersensitivity to silver (Ag).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Buddhist Tzu Chi Medical Foundation Hualien Tzu Chi Hospital
RECRUITINGHualien City, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can spinal stimulation rewire the injured nervous system?
- Implanted nerve stimulator aims to restore walking after spinal injury
- New drug hopes to restore arm function after spinal cord injury
- Spinal implant helps paralyzed patients walk again?
- New at-home device aims to improve bladder control for spinal cord injury patients
- Diabetes drug metformin could help heal spinal cord injuries