Laser light eases shoulder pain in new study
NCT ID NCT07261449
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether low-intensity laser therapy can reduce shoulder pain caused by inflammation of the supraspinatus tendon. Forty adults with confirmed tendinopathy received laser treatment over three months. Researchers measured pain levels, shoulder movement, and quality of life to see if the laser helped.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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40 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Score of 3 or higher on the VAS scale for the shoulder. * Adequate cognitive ability for comprehension. * Rotator cuff tendinopathy confirmed by ultrasound at the study center, either due to tendon inflammation, presence of hypoechoic areas, calcification, fibrillar disorganization, and/or neovascularization in the supraspinatus muscle. * Pain in the proximal lateral part of the arm that worsens with abduction. Exclusion Criteria: * Contraindications specific to laser treatment (e.g., tumors, presence of pacemaker or defibrillator, pregnancy, etc.). * History of glenohumeral fracture and rheumatoid arthritis. * Rheumatic, neurological, or structural polymyalgia affecting the joint. * Previous surgeries. * Pregnant or breastfeeding women. * Taking anticoagulants or antiplatelet agents. * Diabetes mellitus. * Cardiac dysfunction. * Infiltrative and/or rehabilitative treatment in the two months prior to recruitment. * Pre-existing conditions associated with pain in the upper extremities. Difficulties with follow-up. * Depression. * Treatment with another intervention; during the study, they will not be able to undergo it.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Universidad Pontificia de Salamanca
Salamanca, 37002, Spain
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Other studies related to the condition(s) this trial covers.
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