Spinal Cord Stimulation for Intractable Mononeuropathy

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorErasmus Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

Suffering from painful intractable peripheral mononeuropathy in the distal extremities, preferably post-traumatic or post-surgical, confirmed by electromyography (EMG)

Symptoms refractory to conventional medical management for at least 6 months according to treating physician

18 years or older

Pain score on numeric rating scale (NRS) of at least 5 (average pain intensity in week prior to assessment)

Disqualifiers

Mononeuropathy located in the head or torso

Mononeuropathy by avulsion at the plexus brachialis

Life expectancy <1 year

Anticoagulant drug therapy or disturbed coagulation

Trial design

Treatments tested in this trial

  • Spinal cord stimulator

Treatment groups

12 Participants
are divided into 1 treatment group

Sponsors and collaborators

Erasmus Medical Center

Lead sponsor

Boston Scientific Corporation

Collaborator