Skip to main content
Clinical Trials/NL-OMON34598
NL-OMON34598
Recruiting
Not Applicable

Percutaneous nerve stimulation in severe neuropathic pain patients due to spinal cord injury: a feasibility study - Percutaneous nerve stimulation in neuropathic pain due to SCI

Reade, voormalig revalidatiecentrum amsterdam RCA0 sites15 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Reade, voormalig revalidatiecentrum amsterdam RCA
Enrollment
15
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Reade, voormalig revalidatiecentrum amsterdam RCA

Eligibility Criteria

Inclusion Criteria

  • 18 to 70 years of age,
  • SCI at any level and any American Spinal Cord Association (ASIA) impairment Score
  • SCI occurred at least 6 months before inclusion
  • Diagnosis neuropathic pain on the DN4 diagnostic scale (\>\= 4\)
  • At least 6 months of neuropathic pain should be present with a rating of 4 or more on a numeric rating scale from 0 to 10

Exclusion Criteria

  • Pregnancy or planned pregnancy in the study\-period
  • Evidence of significant cardiac conduction disturbance
  • Current or recent substance abuse problem
  • Evidence that would prevent giving informed consent or hinder one\*s ability to follow through with the study based on the attending physicians clinical judgment (e.g. a serious psychological disorder, language difficulties)
  • No informed consent

Outcomes

Primary Outcomes

Not specified

Similar Trials