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Clinical Trials/ISRCTN36818685
ISRCTN36818685Completed未知

Comparison of spinal cord stimulation and the clinical and quantitative sensory testing response in patients with MS pain versus patients with peripheral nerve injury pain

Walton Centre for Neurology and Neurosurgery (UK)0 sites30 target enrollmentStarted: April 23, 2010Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
30

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. Group 1: Confirmed MS with central pain
  • 2. Group 2: Peripheral nerve injury pain
  • 3. Both groups eligible for spinal cord stimulation
  • 4. Group 3: Age- and gender-matched healthy controls
  • 5. Male and female, aged 18 years or older

Exclusion Criteria

  • 1. Unsuitable for spinal cord stimulation
  • 2. High intake of opiates
  • 3. High levels of psychological distress

Investigators

Sponsor
Walton Centre for Neurology and Neurosurgery (UK)

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