Skip to main content
Clinical Trials/NCT04729400
NCT04729400
Completed
Not Applicable

Percutaneous Electrolysis and Vacuum Myofascial Therapy Device in the Treatment of Lateral Epicondylalgia: A Single-Blind Randomized Controlled Trial.

University of Cadiz1 site in 1 country32 target enrollmentJune 10, 2021
ConditionsEpicondylitis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Epicondylitis
Sponsor
University of Cadiz
Enrollment
32
Locations
1
Primary Endpoint
The intensity of pain in epicondylitis
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The concept of epicondylitis refers to the manifestation of pain in the area of insertion of the epicondile muscles, and that it is accompanied by limitation functional. A tendinopathy is characterized as a process of degeneration, with fibroblast proliferation and disorganization of the fibers of collagen. This tendon pathology especially affects the epicondyle extensors and especially the first and second radial and short extensor carpal.

Detailed Description

Experimental group will be treated Therapeutic Percutaneous Electrolysis and Vacuum Myofascial Therapy device once week for four weeks associated with eccentric exercises devices at home and the control group will be included 10 sessions of ultrasound pulsatil therapy (US) and massage associated with eccentric exercises devices at home.

Registry
clinicaltrials.gov
Start Date
June 10, 2021
End Date
October 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Manuel Rodriguez Huguet

Clinical Professor

University of Cadiz

Eligibility Criteria

Inclusion Criteria

  • Patients of both sexes, aged between 18 and 60 years, in an active state of pain and with a diagnosis of one month of evolution.

Exclusion Criteria

  • Patients who are pregnant, have pacemakers and those surgically operated patients who have been treated with electrolysis and Vacuum Myofascial Therapy Device a month earlier

Outcomes

Primary Outcomes

The intensity of pain in epicondylitis

Time Frame: Baseline

A 10-point Numerical Pain Rating Scale (NPRS; 0: no pain, 10: maximum pain) will be used to assess the patients' current level of elbow pain, and the worst and lowest level of pain experienced in the preceding week in the elbow area.

Secondary Outcomes

  • Pressure pain thresholds in epicondylitis trigger points(Baseline, four and twelve weeks)
  • The intensity of pain in epicondylitis(Four and twelve weeks)
  • Active elbow range of motion(Baseline,four and twelve weeks)
  • Questionnaire SF 12(Baseline,four and twelve weeks)
  • Scale PRTEE(Baseline,four weeks and Twelve weeks.)

Study Sites (1)

Loading locations...

Similar Trials