Erasmus Medical Centre
Rotterdam, South Holland, 3015GD, Netherlands
Location status: Recruiting
NCT Number: NCT06546371
Rationale: For patients with mononeuropathy, literature has shown that spinal cord stimulation (SCS) is an effective therapy for patients who are therapy-resistant to more conventional treatments. However, there is a strong need for higher quality evidence to determine the place of this therapy in this target group. Before conducting a large randomized controlled trial (RCT) we propose to conduct an explorative pilot study based on which an effect size estimation and power calculation for a larger study can be done. We will assess the effects of SCS in patients with mononeuropathy measured according to the "Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials" (IMMPACT) guidelines, and assess the stimulation paradigm preferences in these patients.
Objective: To perform an explorative pilot study based on which an effect size estimation and power calculation for an efficacy trial can be done.
Study design: Mono-center explorative pilot study in 12 patients with intractable peripheral mononeuropathic pain who receive a spinal cord stimulator at the Erasmus Medical Centre.
Study population: 12 patients suffering from intractable peripheral mononeuropathic pain.
Intervention: Participants who receive a spinal cord stimulator must fill in IMMPACT guideline questionnaires and undergo several measurement procedures after receiving SCS implantation. The effect of various SCS paradigms on the chronic mononeuropathic pain is assessed at 3 and 6 months.
Main study parameters/endpoints: Effect of 6 months of individually optimized SCS in patients with mononeuropathy according to the IMMPACT guidelines.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Rotterdam, South Holland, 3015GD, Netherlands
Location status: Recruiting
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Electrical stimulation of the dorsal horn to reduce chronic pain.
Time frame: 6 months
Perceived pain intensity as assessed by the brief pain inventory (BPI), with pain scores where 0 is no pain and 10 is worst pain imaginable.
Time frame: 6 months
Quantitative sensory testing (QST) measures sensory thresholds for pain, touch, vibration, and temperature sensations, with the main goal to assess sensory functioning.
Time frame: 6 months
Quality of life as assessed by the EuroQol-5 Dimensions-5 Levels (EQ-5D-5L) questionnaire.
Time frame: 3 months
Perceived pain intensity as assessed by the brief pain inventory (BPI), with pain scores where 0 is no pain and 10 is worst pain imaginable.
Contact information is provided by the study sponsor or research team.
Erasmus Medical Center
Other
Spinal Cord Stimulation for Intractable Mononeuropathy: a Pilot Study
Acronym: SCIMONO
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