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NCT Number: NCT06546371

Spinal Cord Stimulation for Intractable Mononeuropathy

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Erasmus Medical Centre

Rotterdam, South Holland, 3015GD, Netherlands

Location status: Recruiting

Location contact

Mathilde Scholtes, MSc

CONTACT

[email protected]

+31650032165

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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)
  • Stable or absent concomitant analgesics

Exclusion criteria

  • Mononeuropathy located in the head or torso
  • Mononeuropathy by avulsion at the plexus brachialis
  • Life expectancy <1 year
  • Anticoagulant drug therapy or disturbed coagulation
  • Immune-compromised patients
  • Pregnancy
  • Lack of cooperation of the patient or patient has a history of noncompliance with regard to (a) medical regime(s)
  • Patients with psychological factors or addiction that require treatment

Treatment and study plan

Spinal cord stimulator

Device

Electrical stimulation of the dorsal horn to reduce chronic pain.

Primary outcomes

  1. Effect of spinal cord stimulation (SCS) in patients with mononeuropathy as assessed by the perceived pain intensity.

    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.

Secondary outcomes

  1. Effect of SCS in patients with mononeuropathy as assessed by quantitative sensory testing (QST).

    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.

  2. Effect of SCS in patients with mononeuropathy on quality of life.

    Time frame: 6 months

    Quality of life as assessed by the EuroQol-5 Dimensions-5 Levels (EQ-5D-5L) questionnaire.

  3. Patient preferences for SCS paradigms as assessed by the perceived pain intensity.

    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.

Study contacts

Contact information is provided by the study sponsor or research team.

Mathilde Scholtes, MSc

CONTACT

[email protected]

+31650032165

Sponsors and collaborators

Lead sponsor

Erasmus Medical Center

Other

Collaborators

  • Boston Scientific Corporation

Registry information

Official study title

Spinal Cord Stimulation for Intractable Mononeuropathy: a Pilot Study

Acronym: SCIMONO

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 9, 2024
Registry last updated
Mar 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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