CE-STAND: Cervical Epidural STimulation After Neurologic Damage

PHASE1/PHASE2Not yet recruitingINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

October 1, 2025

Primary Completion Date

April 15, 2029

Study Completion Date

April 15, 2029

Conditions
Cervical Spinal Cord Injury
Interventions
DEVICE

Epidural Spinal Cord Stimulation (eSCS)

"The spinal cord stimulator system (Abbott Eterna system implantable pulse generator (IPG), charger, and TriCentrus lead) will be used for this study which is manufactured by Abbott Laboratories. The The stimulators will be surgically inserted above the dura in the spinal canal and administer an electrical signal from the neurostimulator to specific sections of the spinal cord underlying the electrodes. The duration of implantation will be 10 years (the longevity of the device battery). The device will not be removed unless it causes complications such as malfunction, illness, or other harm.~The device can also be removed electively for any reason."

All Listed Sponsors
lead

University of Minnesota

OTHER

NCT06410001 - CE-STAND: Cervical Epidural STimulation After Neurologic Damage | Biotech Hunter | Biotech Hunter