Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
ID07247825

Efficacy of Therapeutic Percutaneous Electrolysis vs Laser Therapy in Supraspinatus Tendinopathy Randomized Clinical Trial

Led by Universidad Pontificia de Salamanca · Updated on 2026-05-04

40

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Supraspinatus tendinopathy is a common cause of shoulder pain and functional problems, especially affecting people who perform repetitive work above shoulder height or play sports involving overhead movements. This trial investigates the effects of two treatments: therapeutic percutaneous electrolysis and laser therapy, to compare their impact on this condition. The study is a single-blind randomized clinical trial recruiting patients diagnosed by an orthopaedic surgeon and confirmed with ultrasound imaging. Participants will receive one of two treatments targeting the supraspinatus tendon. The electrolysis group undergoes an invasive procedure where an ultrasound-guided needle delivers galvanic current to the affected tendon area for 1 minute and 20 seconds. The laser therapy group receives non-invasive laser treatment on the same tendon. Both treatments are administered at the ValleSur physiotherapy clinic, with evaluations conducted before, immediately after, 24 hours after, and one week post-intervention. During the study, participants will be assessed for pain intensity, range of motion, and quality of life related to their shoulder condition. Ultrasound imaging guides treatment and evaluates the tendon. The trial monitors short- and medium-term effects up to one week after treatment. The total participation time includes treatment and follow-up assessments over this one-week period.

CONDITIONS

Brief Title

Efficacy of Therapeutic Percutaneous Electrolysis vs Laser Therapy in Supraspinatus Tendinopathy.

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Signed informed consent to participate and undergo invasive physiotherapy techniques
  • Symptoms such as inflammation or pain lasting 4 weeks or more
  • Positive palpation test of the supraspinatus tendon
  • Men and women aged 18 to 65 years
  • Shoulder pain analogue scale score of 3 or higher
  • Adequate cognitive ability to understand the study
  • Limited shoulder range of motion
  • Supraspinatus tendinopathy confirmed by ultrasound showing inflammation, hypoechoic areas, calcification, fibrillar disorganisation, or neovascularisation
  • Pain in the upper outer arm worsening with arm abduction
Not Eligible

You will not qualify if you...

  • Any acute or chronic musculoskeletal disease affecting study results
  • Neuropathic pain like lumbar radiculopathy
  • Failure to attend treatment sessions or assessments
  • History of glenohumeral fracture or rheumatoid arthritis
  • Rheumatic, neurological, or structural polymyalgia affecting the joint
  • Pregnancy
  • Cardiovascular disease
  • Neurological disease
  • Local infection
  • Tumours
  • Belonephobia (fear of needles)
  • Use of anticoagulants or antiplatelet agents
  • Infiltrative or rehabilitative treatment within 2 months before recruitment
  • Receiving other interventions during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Implementation

Duration - 1 week

Participants receive either therapeutic percutaneous electrolysis or laser treatment on the supraspinatus tendon.

1 to 2 visits depending on treatment assignment

Trial Site Locations

Total: 1 location

1

Universidad Pontificia de Salamanca

Salamanca, Spain, 37002

Actively Recruiting

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Research Team

J

Jorge V Velázquez Saornil, PhD.

J

Jorge Velázquez Saornil, PhD.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Relationship between chronic pathologies of the supraspinatus tendon and the long head of the biceps tendon: systematic review.

Lucía Redondo-Alonso, Gema Chamorro-Moriana, José Jesús Jiménez-Rejano...

https://pubmed.ncbi.nlm.nih.gov/25408141

Effectiveness of physical therapy treatment of clearly defined subacromial pain: a systematic review of randomised controlled trials.

M N Haik, F Alburquerque-Sendín, R F C Moreira...

https://pubmed.ncbi.nlm.nih.gov/27288517

Current advances and novel research on minimal invasive techniques for musculoskeletal disorders.

Carlos Romero-Morales, María Bravo-Aguilar, Vanesa Abuín-Porras...

https://pubmed.ncbi.nlm.nih.gov/34099238

Efficacy of percutaneous electrolysis for the treatment of tendinopathies: A systematic review and meta-analysis.

Laura Asensio-Olea, Raquel Leirós-Rodríguez, Mª Pilar Marqués-Sánchez...

https://pubmed.ncbi.nlm.nih.gov/36583575

Changes in Gene Expression Associated with Collagen Regeneration and Remodeling of Extracellular Matrix after Percutaneous Electrolysis on Collagenase-Induced Achilles Tendinopathy in an Experimental Animal Model: A Pilot Study.

José Luis Sánchez-Sánchez, Laura Calderón-Díez, Javier Herrero-Turrión...

https://pubmed.ncbi.nlm.nih.gov/33076550