Skip to main content
Clinical Trials/NCT05097937
NCT05097937CompletedNot Applicable

Neurophysiological Effects of Percutaneous Electrolysis Related to Endogenous Pain Modulation

University of Salamanca2 sites in 1 country54 target enrollmentStarted: November 22, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
54
Locations
2
Primary Endpoint
Changes from baseline in Pressure Pain Thresholds (PPT)

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Basic Science
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Sergio Varela Rodríguez

PhD candidate

University of Salamanca

Study Sites (2)

Loading locations...

Similar Trials