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Study identifier: NCT07413731 Synced from ClinicalTrials.gov · July 29, 2026
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Neurophysiological Effects of Medication Tapering During Treatment With Spinal Cord Stimulation

Condition: Persistent Spinal Pain Syndrome Type 2 (PSPS-T2), Lower Spine · Spinal Cord Sensitivity to Neurostimulation · Neurophysiological Sensitivity to Spinal Cord Stimulation  ·  Sponsor: Brai²n

PhaseN/A
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is being conducted in patients who will receive a spinal cord stimulator. This device helps manage chronic neuropathic pain in the trunk and/or limbs. The patients will receive a spinal cord stimulator that is available, notified, and reimbursed in Belgium, which uses a special technology automatically adjusting the intensity of the stimulation. This is called a closed-loop system. The closed-loop system stimulates the Beta fibers in the spinal cord and simultaneously measures their response. Based on the measured response, the stimulation strength is automatically adjusted. In Belgium, after implant of the leads the effect must first be evalauted for 3 weeks before implanting the Internal Pulse Generator; this is called the trial period. Only if the trial is successful, the patients will receive a permanent implant. The primary goal of the study is to evaluate how different types of pain medication influence the neurophysiological response of the Beta fibers during spinal cord stimulation. Patients will be divided into three groups, based on the medication they are taking before receiving a spinal cord stimulator: * patients not taking any pain medication, * patients taking strong opioids, * patients taking anticonvulsant medication. As part of the study, patients will follow the normal clinical schedule. During visits, they will be asked questions about their pain, sleep, medication use, and activity. The study will end one month after the patient receives th…

This description comes directly from the study's public registry record.

Talk to the study team

Pieter Van Looy  ·  +32 3 443 48 72  ·  pieter.vanlooy@zas.be

Always discuss trial participation with your own doctor first.

Locations (1)

Brai²n - ZAS AugustinusWilrijk, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT07413731