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Clinical Trials/NCT02559999
NCT02559999
Completed
Not Applicable

Objective Markers of Pain Perception in Humans: a Study in Healthy Subjects

Centre Hospitalier Universitaire de Saint Etienne2 sites in 1 country21 target enrollmentJune 4, 2014
ConditionsHealthy

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Enrollment
21
Locations
2
Primary Endpoint
EEG Gamma power.
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Determine objective markers of pain perception remains a major scientific and medical issue. Various tools have been proposed to objectify pain, but their adaptability to different clinical contexts are limited. Our working hypothesis considers that the research for markers of immediate pain perception should be based on an electrophysiological approach, based on the combined analysis of EEG and autonomic responses.

Detailed Description

This project aims to study the cortical and autonomic responses induced by tonic painful stimulation compared to those induced by comparable sensory and stressful stimulations, by combining high density EEG, cutaneous sympathetic, cardiovascular and pupillary recordings.

Registry
clinicaltrials.gov
Start Date
June 4, 2014
End Date
February 28, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Affiliate or beneficiary of social security
  • Signature of consent

Exclusion Criteria

  • History of cardiovascular disease (vagal syncope, hypertension, etc ...), renal, metabolic (diabetes ...), psychiatric (depression, etc ...) or neurological (seizure, etc ...) syndromes;
  • Reynaud's syndrome;
  • Raynaud's disease;
  • Acrocyanosis;
  • Known rhythm disorders;
  • Participation at the same time in another clinical trial;
  • Taking a medical treatment;
  • Suffering from acute (complaint of pain in the week before the test) or chronic pain,
  • Allergic to conductive gel for electrodes.

Outcomes

Primary Outcomes

EEG Gamma power.

Time Frame: Baseline

The EGG signals are compared between a painful stimuli tonic to those evoked by non-painful stimuli.

Secondary Outcomes

  • Magnitude of the sympathetic cutaneous reactivity(Baseline)
  • Amplitude of pupillary dilation(Baseline)
  • ratio of low to high frequency spectral powers(Baseline)

Study Sites (2)

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