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Effectiveness of Percutaneous Electrolysis in the Treatment of Lateral Epicondylalgia. A Single-Blind Randomized Controlled Trial.

Effectiveness of Percutaneous Electrolysis in the Treatment of Lateral Epicondylalgia. A Single-Blind Randomized Controlled Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03225404
Acronym
MRH
Enrollment
32
Registered
2017-07-21
Start date
2018-07-18
Completion date
2018-09-18
Last updated
2022-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epicondylitis

Keywords

Tendinopathy, Electrolysis, Exercise, Dry needing

Brief summary

The concept of epicondylitis refers to the manifestation of pain ni the area of insertation of the epicondile muscles, and that it is accompained by limitation funcional.A tendinopathy is characterized as a process of degenaration, 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

Eccentric exercises of the epicondyle muscles were performed in 3 sets of 10 repetitions. Participants were asked to perform the exercise program on an individual basis twice every day for 4 weeks. The eccentric program consisted of 3 exercises, focusing on the epicondyle muscles. Participants were asked to do a normal flexion extension (concentric phase) and a slow return to the initial position (eccentric phase) included first the concentric phase, and the eccentric phase was slowly conducted. The exercise program was taught by a physiotherapist in the first session and monitored in the subsequent sessions.

Interventions

OTHEREpte group

Therapeutic Percutaneous Electrolysis once week for four weeks associated with eccentric exercises devices at home.

The intervention for this group consisted of dry needling in trigger points associated with eccentric exercises devices at home.

Sponsors

University of Cadiz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Outcomes assesor

Intervention model description

A specialist physician will be diagnosed the epicondylitis

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

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 Epte a month earlier

Design outcomes

Primary

MeasureTime frameDescription
The intensity of pain in epicondylitisBaselineA 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

MeasureTime frameDescription
The intensity of pain in epicondylitisFour and twelve weeksA 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.
Active elbow range of motionBaseline,four and twelve weeksMeasured by a two branches egoniomter
Pressure pain thresholds in epicondylitis trigger pointsBaseline, four and twelve weeksPressure pain thresholds (PPTs) will be measured with a pressure algometer (Baseline)
Questionnaire SF 12Baseline,four and twelve weeksThe multidimensional health related quality of life

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026