New nerve block combo may offer safer pain relief for shoulder surgery
NCT ID NCT07689045
First seen Jul 07, 2026 · Last updated Jul 09, 2026 · Updated 2 times
Summary
This trial tests whether a combination of two nerve blocks (Modified PENG and Suprascapular) can control pain after shoulder surgery as well as the standard interscalene block, but with fewer side effects like breathing trouble or muscle weakness. About 70 adults having Bankart repair or Latarjet surgery will be randomly assigned to one of the two methods. The main goal is to compare pain levels 24 hours after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Modified PENG Block combined with Suprascapular Nerve Block
- What this could lead to
- If successful, this approach could offer a safer alternative for pain control after shoulder surgery, reducing breathing problems and muscle weakness.
- What could go wrong
- This is a small, early-stage trial. The new block may not control pain as well as the standard method, and results may not apply to 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 70 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Nov 2026
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 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: * • Male or female patients aged 18 to 65 years. * Patients undergoing elective Bankart repair or Latarjet surgery. * American Society of Anesthesiologists (ASA) physical status I or II. Exclusion • Patient refusal. * History of allergy to local anesthetics. * Chronic opioid use (\>3 months). * Coagulation disorders. * Pre-existing neurological or musculoskeletal disorders. * Respiratory compromise (e.g., COPD)
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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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Faculty of Medicine , Cairo University Hospitals
RECRUITINGCairo, Cairo Governorate, Egypt
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