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Clinical Trials/NL-OMON34703
NL-OMON34703
Completed
N/A

Quantitative sensory testing (QST) protocol. - QST procedure

PRA International EDS0 sites400 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
PRA International EDS
Enrollment
400
Status
Completed
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
PRA International EDS

Eligibility Criteria

Inclusion Criteria

  • Patients with chronic pain
  • Gender: male and female
  • Age: between 18 and 80 years of age, inclusive
  • Pathology: chronic pain history of 3 months or longer
  • pain has been considered by a physician to be either of neuropathic origin, or resulting from nerve damage due to diabetes mellitus, of postherpetic neuralgia, of phantom pain (i.e., pain resulting from an amputed limb)
  • Weight: no specific criteria;Healthy volunteers
  • Gender: male and female
  • Age: between 18 and 80 years of age, inclusive
  • Weight: no specific criteria

Exclusion Criteria

  • Patients with chronic pain:
  • \- mental handicap;Healthy volunteers:
  • \- history of chronic pain
  • \- history of neurological disorders
  • \- history of psychiatric disorders
  • \- regular use of pain medication

Outcomes

Primary Outcomes

Not specified

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