Shoulder pain study: brain sensitivity may predict injection success
NCT ID NCT05926895
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at 44 people with shoulder pain from rotator cuff tears to see if a condition called central sensitization (where the nervous system is extra sensitive to pain) changes how well a steroid injection works. Participants got a shot of betamethasone and prilocaine into the shoulder, and researchers measured pain and movement. The goal was to find out if those with central sensitization respond differently, which could help tailor treatments in the future.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Betamethasone and prilocaine injection
- What this could lead to
- If it works, this could help doctors predict which patients will benefit from steroid injections for shoulder pain, leading to more personalized treatment.
- What could go wrong
- This is a small, completed study (44 people) that only looks for a link, not a treatment. Results may not apply to everyone with shoulder pain.
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
-
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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44 people
The number who actually took part.
- Started
-
Jun 2023
- Finished
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Dec 2024
- Lead sponsor
-
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.
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: * Rotator cuff pathology confirmed clinically and radiologically (USG/MRI) * Failure to respond to medical/physical treatment * Agree to participate in the study Exclusion Criteria: * Shoulder trauma and history of previous shoulder surgery * History of injection to the painful shoulder in the last 3 months * Use of centrally acting drugs (antidepressants, pregabalin, gabapentin and myorelaxant etc.) * History of active cancer, systemic inflammatory disease, and infection * 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.
Contacts and locations
Locations
-
Sultan Abdülhamid Han Research and Training Hospital
Istanbul, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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