New nerve block techniques may protect breathing during shoulder surgery recovery
NCT ID NCT05920421
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested two newer nerve block methods for shoulder surgery pain relief, aiming to avoid a common side effect: temporary paralysis of the diaphragm, the main breathing muscle. 87 adults having shoulder surgery received one of three types of nerve blocks. The researchers measured diaphragm movement and pain levels to see if the newer blocks were safer and still effective.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nerve blocks (subomohyoid infraclavicular, subomohyoid subscapularis, interscalene)
- What this could lead to
- If successful, these alternative nerve blocks could provide effective pain relief for shoulder surgery while lowering the risk of temporary diaphragm paralysis.
- What could go wrong
- This is a small, completed study (87 people) comparing different techniques. Results may not apply to all patients or surgeries, and the blocks may still carry some risk of diaphragm issues.
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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87 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Dec 2024
- Lead sponsor
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A government agency
The lead sponsor is a government body.
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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21 to 60 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: * Patient acceptance. * ASA I and ASA II. * Age 21-60 years old. * Both gender. * BMI \< 35 Kg/m2. * Accepted mental state of the patient. * Elective Unilateral upper limb surgeries at the level of the shoulder. * Time of surgery less than 2 hours Exclusion Criteria: * \- Patient refusal. * Peripheral neuropathy. * Pathological coagulopathy. * Infection at the injection site. * Untreated pneumothorax. * Disturbed conscious level. * An allergy to local anesthetics used in this study
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Genom att skicka in godkänner du våra Användarvillkor
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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Emad Hamdy Mohamed Morsy
Zagazig, Sharqia Province, 44519, Egypt