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Clinical Trials/NCT02531048
NCT02531048
Completed
Not Applicable

Normative Values Laser Nociceptive Evoked Potentials Depending on the Age

Centre Hospitalier Universitaire de Saint Etienne1 site in 1 country120 target enrollmentFebruary 2008
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
120
Locations
1
Primary Endpoint
composite outcomes : latencies (ms) and amplitudes (μV) of nociceptive evoked potential
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Different neurological damage may alter the pain conduction systems centrally (spinothalamic pathway) or peripherally (small caliber sensory fibers A delta and C). The laser thermal stimulation selectively stimulates the pain pathways and generates nociceptive signals conveyed to the cortex. Registering these cortical responses constitute the technical laser nociceptive evoked potentials. If these tests are routinely used, their interpretation must remain cautious especially in the elderly.

Detailed Description

Different neurological damage may alter the pain conduction systems centrally (spinothalamic pathway) or peripherally (small caliber sensory fibers A delta and C). The laser thermal stimulation selectively stimulates the pain pathways and generates nociceptive signals conveyed to the cortex. Registering these cortical responses constitute the technical laser nociceptive evoked potentials. If these tests are routinely used, their interpretation must remain cautious especially in the elderly. Normal values that are available have been obtained in young subjects. However, various studies have shown that the integration of nociceptive messages depended on age. The aim of this study was to establish normal values of nociceptive evoked potentials for each age group of 18 to 75 years.

Registry
clinicaltrials.gov
Start Date
February 2008
End Date
December 2013
Last Updated
2 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Neurological history
  • Neuralgia history (\> 3 months)
  • Pathology can cause neuropathy (unbalanced thyroid dysfunction, diabetes, kidney failure, chronic hepatitis, HIV ...)
  • Dermatological disorder known type of Lucite or photosensitivity
  • Medical treatment analgesic, psychotropic or anti-epileptic underway
  • Toxic acquired in the last 72 hours (alcohol, cannabis, other toxic ...)
  • Pregnant women
  • Incapacitate to stand still
  • Participation in another biomedical research in the field of pain in the three months prior to inclusion.

Outcomes

Primary Outcomes

composite outcomes : latencies (ms) and amplitudes (μV) of nociceptive evoked potential

Time Frame: Day 0

Secondary Outcomes

  • detection threshold (mJ/mm2)(Day 0)
  • nociceptive threshold (mJ/mm2)(day 0)

Study Sites (1)

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