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Effects of Spinal Cord Stimulation on Sensory Perceptions of Chronic Pain Patients

CompletedNot applicableNCT02837822
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

It's well known that Spinal cord stimulation (SCS) changes the perception of chronic pain in the area stimulated by epidural electrodes. However, we don't know the effect of this type of stimulation on the perception of external sensations (temperature, touch, pressure, and vibration) and sharp pain. Quantitative sensory testing (QST) is used to quantify somatosensory phenotype. This QST battery tests different subtypes of nerve fibres (Aβ, Aδ and C) involved in the transduction of sensory information from the periphery to the spinal cord. The purpose of this study is to evaluate the effects of the SCS on sensory perceptions of patients with chronic pain (CRPS, FBSS). Sensorial perception tests will be carried out in accordance with a standardized procedure (Rolke et al. Pain, 2006). For non-implanted patients, an initial visit will be conducted before the operation. For all participants, two other visits will take place at least 6 months after the operation to perform the tests with and without stimulation.

Study details

Official title
Effects of Spinal Cord Stimulation on Sensory Perceptions of Chronic Pain Patients
Interventions
Sponsor
CHU de Quebec-Universite Laval
Start date
2015-10
Primary completion
2018-05
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Canada, United States
Total sites listed
2

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Participant with a diagnosis of CRPS or FBSS that meet International Association for the Study of Pain's criteria; * Pain in one leg; * Paresthesia area limited to the treated leg; * No changes in the programming patterns of the device for a minimum of 30 days before the tests; * Informed consent. Exclusion Criteria: \- Wounds or infections at the painful site.

Canadian sites (1)

FacilityCityProvince
CHU de Québec - Université LavalQuébec

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02837822