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/Actively Recruiting
Led by Universidad Pontificia de Salamanca · Updated on 2026-07-07
40
Participants Needed
1
Research Sites
13 weeks
Total Duration
Supraspinatus tendinopathy is a common cause of shoulder pain and functional problems, especially worsened by repetitive overhead work or sports. This trial evaluates the short- and medium-term effects of two types of therapeutic percutaneous electrolysis treatments guided by ultrasound compared to laser therapy. It is a single-blind, randomized clinical trial involving patients diagnosed by an orthopedic surgeon and selected based on specific clinical and imaging criteria. Participants will receive either simple or multifilar electrolysis treatment applied invasively under ultrasound guidance. The procedure involves positioning the patient, cleaning the area, localizing the target tissue with ultrasound, and applying controlled galvanic current using a specialized device. Each treatment session lasts about 1 minute and 20 seconds at a set intensity. The study includes four evaluations before treatment, immediately after, 24 hours later, and one week after intervention. During the study, participants will be assessed for pain intensity, shoulder range of motion, and quality of life at one week after treatment. Evaluations include clinical examination and ultrasound imaging. The trial monitors these outcomes to compare the effectiveness of the electrolysis methods. The total study duration includes treatment and follow-up assessments within one week from intervention, with completion scheduled by August 2026.
CONDITIONS
Efficacy of Therapeutic Percutaneous Electrolysis Simple vs Multifiliar Therapy in Supraspinatus Tendinopathy.
J
Jorge V Velázquez Saornil, PhD.
J
Jorge Velázquez Saornil, PhD.
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Universidad Pontificia de Salamanca
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single session
Participants receive either simple or multifilar percutaneous electrolysis treatment guided by ultrasound.
1 visit (in-person)
Duration - 1 week
Participants are evaluated before treatment, immediately after, 24 hours later, and one week after intervention to assess pain, shoulder motion, and quality of life.
4 visits (in-person)
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Lucía Redondo-Alonso, Gema Chamorro-Moriana, José Jesús Jiménez-Rejano...
https://pubmed.ncbi.nlm.nih.gov/25408141/Carlos Romero-Morales, María Bravo-Aguilar, Vanesa Abuín-Porras...
https://pubmed.ncbi.nlm.nih.gov/34099238/M N Haik, F Alburquerque-Sendín, R F C Moreira...
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https://pubmed.ncbi.nlm.nih.gov/36583575/José Luis Sánchez-Sánchez, Laura Calderón-Díez, Javier Herrero-Turrión...
https://pubmed.ncbi.nlm.nih.gov/33076550/Universidad Pontificia de Salamanca
Lead Sponsor