Why do some shoulder injections work better? a study looks for clues in pain type
NCT ID NCT07792421
First seen Aug 28, 2026 · Last updated Sep 03, 2026 · Updated 2 times
Summary
This study follows 134 adults with subacromial pain syndrome, a common cause of shoulder pain. All receive a routine corticosteroid injection into the shoulder as part of usual care. Researchers test whether people with a nociplastic pain phenotype, a type of pain processing that is not purely tissue-based, experience a different change in pain four weeks after the injection compared to those without this phenotype. The goal is to see if a simple pain assessment can help predict who benefits most from this standard treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Corticosteroid injection into the shoulder, given as part of routine care
- What this could lead to
- If pain phenotype predicts response, doctors could tailor shoulder pain treatment, offering injections to those most likely to benefit and alternatives to others.
- What could go wrong
- This observational study does not test a new treatment; it only looks for a link. The results may not apply to all patients, and the injection itself carries typical risks like temporary pain or infection.
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.
- Participants
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About 134 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2028
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.
Who is studied
Patients referred to and evaluated at the specialised shoulder clinic at Vejle Hospital, Denmark
- Ages
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18 to 70 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: 1. Diagnosed with SAPS (dm751, dm753, dm754, dm755 2. Shoulder pain ≥ 3 months 3. ≥ 3 out of 5 specific shoulder test 4. Age 18-70 years 5. Increased pain during active arm elevation 6. Pain during active elevation ≥ 3 (VAS) 7. Receving a corticosteroid injection based on routine clinical proctice Exclusion Criteria: 1. Severe visual impairment 2. Epilepsy 3. Severe cognitive or physical impairment 4. Language barrier (Danish) 5. Receving a corticosteroid injection at a site other than the subacromial bursa (e.g. acromioclavicular joint or intra-articular injection)
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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 places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Vejle Hospital
Vejle, Denmark
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