Skip to main content
Clinical Trials/NCT03169049
NCT03169049
Unknown
Not Applicable

Peripheral Nerve Conduction Block Using a High Frequency Alternating Stimulation: A Pilot Study

University of Castilla-La Mancha0 sites10 target enrollmentJuly 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Nerve Block
Sponsor
University of Castilla-La Mancha
Enrollment
10
Primary Endpoint
Hand muscle strength after treatment 20 min
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to determine whether the transcutaneous application of unmodulated high frequency alternating currents could produce a quickly conduction block of peripheral nerve.

Detailed Description

In the last years several animal experimental studies have evidenced that high frequency unmodulated currents about 5 KHz can cause a peripheral nerve block. However electric currents with these high frequencies that are usually used for the treatment of pain in humans are interrupted or modulated (i.e. interferential currents). It has show that the diameter of the nerve it is related with the frequency to produce the conduction block. For this reason the investigators decided to applied 20KHz to observe the effects on maximal manual force and to compare versus sham stimulation. Only one study has applied 5KHz on experimental pain and they have demonstrated changes in somatosensory thresholds.

Registry
clinicaltrials.gov
Start Date
July 2017
End Date
September 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University of Castilla-La Mancha
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Healthy volunteers

Exclusion Criteria

  • Neuromuscular disease.
  • Epilepsy.
  • Trauma, surgery or pain affecting the upper limb, shoulder girdle or cervical area.
  • Osteosynthesis material in the upper limb.
  • Diabetes.
  • Cardiovascular disease.
  • Pacemaker or other implanted electrical device.
  • Take any drug (NSAIDs, corticosteroids, antidepressants, analgesics, antiepileptics, ...) during the study and in the previous 7 days.
  • Presence of tattoos or other external agent introduced into the treatment or assessment area.
  • Pregnancy

Outcomes

Primary Outcomes

Hand muscle strength after treatment 20 min

Time Frame: After treatment 20 min

The hand muscle strength will be measured with a dynamometer and will be expressed in Newton

Baseline Hand Muscle Strength

Time Frame: Baseline at 0 min

The hand muscle strength will be measured with a dynamometer and will be expressed in Newton

Secondary Outcomes

  • Change from baseline in Muscle strength(baseline at 0 min, immediately after treatment at 20 min)

Similar Trials