Clinical Trial

Brain-controlled Spinal Cord Stimulation in Participants With Chronic Stroke for Lower and Upper Limb Rehabilitation

Study acronym: Stroke-BSI
Recruiting
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Summary
The purpose of this clinical study is to evaluate the preliminary safety and effectiveness of using a cortical recording device (ECoG) combined with cervical and lumbar targeted epidural electrical stimulation (EES) of the spinal cord to restore voluntary motor functions of upper and lower limbs in participants with chronic stroke suffering from mobility impairment. The goal is to establish a direct bridge between the motor intention of the participant and the spinal cord, which should not only improve or restore voluntary control of arm and leg movement and support immediate mobility, but also promote neurological recovery when combined with neurorehabilitation.
Protocol Amendment History 3 changes
critical Recruitment opened 2026-06-09
notable Primary completion pushed: 2028-04 -> 2028-10 2026-06-09
minor Completion pushed: 2032-04 -> 2032-10 2026-06-09
Trial Details
NCT Number NCT07610850
Lead Sponsor Ecole Polytechnique Fédérale de Lausanne
Conditions Stroke, Hemiplegia
Enrollment 3 participants
Start Date 2026-09-01
Primary Completion 2028-10 (estimated)
Study Completion 2032-10 (estimated)
Updated on ClinicalTrials.gov 2026-06-08