Epidural Stimulation for Upper Extremity Function

Technology

Arm/hand function

Online since 15 October 2024, updated 6 days ago

About this trial

This trial is enrolling 20 participants with cervical spinal cord injury who have undergone nerve transfer surgery at least 6 months ago, to test the effect of epidural spinal cord stimulation (SCS) on hand and arm function. SCS is a technique for stimulating the spinal cord; in this case, temporary SCS leads will be imlanted under the skin in the cervical spine region above the injury area. If included, participants will receive SCS for 4 weeks. Final testing of hand and arm function will be performed after 6 weeks.

Included participants

Gender

All

Age

18 - 65 years

Injury level

C1 - T1

Severity (AIS)?

Time since injury

All

Healthy volunteers

C1-T1

Additionally, participants must

NOT have a functional implanted device (pacemaker, vagus nerve device, baclofen pump)

have had upper extremity nerve transfer > 6 months prior to enrollment

What’s involved

Type

Technology

Details

- Participants will receive epidural spinal cord stimulation (SCS) for 4 weeks. - SCS is a technique for stimulating the spinal cord to modify spinal cord function. This study uses percutaneous leads which are inserted in the cervical region of the spine. - Final testing of hand and arm function will be performed after 6 weeks.

Potential benefits

Main benefits

Arm/hand function

Additional benefits

General health

Pain

Good to know: Potential benefits are defined as outcomes that are being measured during and/or after the trial.

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