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Clinical Trials/NCT05097937
NCT05097937
Completed
Not Applicable

Neurophysiological Effects of Percutaneous Electrolysis Related to Endogenous Pain Modulation

University of Salamanca1 site in 1 country54 target enrollmentNovember 22, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Percutaneous Electrolysis
Sponsor
University of Salamanca
Enrollment
54
Locations
1
Primary Endpoint
Changes from baseline in Pressure Pain Thresholds (PPT)
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Percutaneous electrolysis is based on the application of a galvanic current through an acupuncture needle. The underlying mechanisms that explain the efficacy of this technique are not completely well understood. The objective is to delve into the neurophysiological analgesic effects of percutaneous electrolysis. Participants will be assigned to one of three intervention groups. The analgesic effects of the technique will be evaluated by means of variables related to endogenous pain modulation.

Registry
clinicaltrials.gov
Start Date
November 22, 2021
End Date
February 11, 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Sergio Varela Rodríguez

PhD candidate

University of Salamanca

Eligibility Criteria

Inclusion Criteria

  • Asymptomatic subjects
  • Signature of the informed consent

Exclusion Criteria

  • Fear of needles
  • Any pathology or process that causes pain
  • Neurological, rheumatologic, cardiovascular or metabolic diseases
  • Cutaneous alterations and cognitive or sensitivity disorders
  • Pregnancy
  • Recent intake of alcohol or caffeine
  • Vigorous physical activity on the day of testing

Outcomes

Primary Outcomes

Changes from baseline in Pressure Pain Thresholds (PPT)

Time Frame: Baseline and immediately after the intervention

PPTs will be measure by algometry in the common extensor tendon of the epicondyle, bicipital groove and tibialis anterior muscle (all of the right side).

Secondary Outcomes

  • Changes from baseline in Temporal Summation (TS)(Baseline and immediately after the intervention)
  • Changes from baseline in Conditioned Pain Modulation (CPM)(Baseline and immediately after the intervention)

Study Sites (1)

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