About this trial
Patients suffereing from chronic pain due to persistent spinal pain syndromes or complex regional pain syndromes and living in Belgium will be included in this register once they are being considered for a treatment with invasive neuromodulation (either spinal cord stimulation either dorsal root ganglion stimulation). The screening process, the multidisciplinary evaluation, the trial therapy and the long-terl follow-up will be monitored through this register.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
chronic pain syndromes
Disqualifiers
acute pain syndromes
Trial population
Adult patients suffering from chronic pain syndromes, either persistent spinal pain syndromes or complex regional pain syndromes.
Trial design
Cohort
Prospective
Treatments tested in this trial
Spinal cord stimulation
Procedure/Surgeryimplantation of electrode which is linked to an implantable impulse generator for the treatment of chronic pain syndromes.
Treatment groups
Trial outcomes
Primary outcomes
Pain intensity after 21 days
Follow-up of pain intensity (measured by the Numeric Rating Scale, with a minimum of 0 and a maximum score of 10) during the trial therapy of 21 days, together with quality of sleep and quality of ambulation (also ona NRS scale from 0 to 10).
Sponsors and contacts
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