Shoulder surgery pain study: which nerve block works best?
NCT ID NCT05442814
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two methods of numbing the suprascapular nerve (a nerve in the shoulder) to control pain after arthroscopic shoulder surgery. Sixty adults scheduled for shoulder surgery received either an anterior or posterior nerve block. Researchers measured pain levels, diaphragm movement, and opioid use to see which approach was safer and more effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Suprascapular nerve block (a numbing injection near the shoulder nerve)
- What this could lead to
- If one approach works better, it could mean less pain and fewer breathing side effects after shoulder surgery.
- What could go wrong
- This is a small, completed study with only 60 people, so results may not apply to everyone. Both methods are already used, so no big breakthrough is expected.
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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60 people
The number who actually took part.
- Started
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Jul 2022
- Finished
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Jul 2023
- 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 80 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: * Patient who accepts to study protocol * Scheduled for shoulder surgery * Between the ages of 18 and 80 Exclusion Criteria: * Patients with coagulopathy * Patients with a history of local anesthetic drug allergy and toxicity * Patients with advanced organ failure * Patients with mental retardation * Patients with infection present at the injection site * Patients with diaphragm paralysis * Pregnant patients
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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
-
Istanbul Medeniyet University
Istanbul, 34722, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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