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Effects of Spinal Cord Stimulation

Not Applicable
Recruiting
Conditions
Chronic Pain
Interventions
Device: Spinal cord stimulation turned on with suggestions (suggestions on)
Registration Number
NCT05885061
Lead Sponsor
University of Aarhus
Brief Summary

The goal of this interventional study is to test effects of spinal cord stimulation in patients receiving treatment for their chronic pain. The main question of the study is:

• What is the effect of spinal cord stimulation when compared to placebo? Participants will rate their pain with their usual spinal cord stimulation on and off.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
25
Inclusion Criteria
  • Patients (>18 years of age) with SCS implanted to treat chronic pain.
  • Patients who consent to participation and can cooperate in the study.
  • Use of continuous paresthesia-free SCS for minimum 6 months prior to participation in the study.
  • Pain score of 7 or less on a 0-10 scale in the most painful area treated with SCS, rated upon inclusion.
  • Patients not receiving other neuromodulation treatment.
  • Patients who have not undergone changes in their (pain relevant) medication during the last 30 days (pro necessitate medication allowed).
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Spinal cord stimulation turned on and suggestionsSpinal cord stimulation turned on with suggestions (suggestions on)-
Primary Outcome Measures
NameTimeMethod
Pain intensity, Visual Analogue ScaleEvery 30 minutes during study session (max 5 hours)

0-10 (0=no pain, 10=worst imaginable pain). Continual assessments to register changes.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Department of Neurosurgery, Aarhus University Hospital

🇩🇰

Aarhus, Denmark

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