Laser vs shock wave: which zaps shoulder pain better?
NCT ID NCT07667998
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will compare two non-invasive treatments—high-intensity laser therapy and extracorporeal shock wave therapy—for people with chronic supraspinatus tendinopathy (a common shoulder tendon condition). Researchers will measure tendon thickness, shoulder space, pain, range of motion, and hand strength in 69 adults aged 18 to 50. The goal is to find which therapy works better to ease symptoms and improve function.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- High-intensity laser therapy and extracorporeal shock wave therapy
- What this could lead to
- If this trial succeeds, it could show which non-invasive therapy better reduces tendon thickness and improves shoulder pain and function.
- What could go wrong
- This is a small, early-stage study with only 69 participants, so results may not apply to everyone. Both treatments are non-invasive but may not work for all patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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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About 69 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- 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 50 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients from 18 to 50 years old of both genders. * Unilateral Chronic Supraspinatus Tendinitis in dominant side * BMI 18.5-24.9 * Tenderness is found over the supraspinatus as it passes subacromial and anterolateral The patient will report pain with active shoulder elevation in the scapular plane (eg: welders, plate workers, slaughterhouse workers and overhead playing athletes) * The patient will report pain with resisted isometric abduction. * The patient will report positive Jobe's test (empty can test) Exclusion Criteria: * Post shoulder surgery, traumatic incidents * Partial tears at surgery * Massive retracted tears at surgery * Frozen shoulder Rotator cuff tear * Glenohumeral or acromioclavicular arthritis * Implanted pacemaker * Pregnancy
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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