New nerve block may keep arm strong after shoulder surgery
NCT ID NCT07057947
First seen Jun 30, 2026 · Last updated Jul 01, 2026 · Updated 1 time
Summary
This trial tests whether a newer type of nerve block, called the pericapsular nerve group (PENG) block, can control pain during shoulder arthroscopy without weakening the arm muscles as much as the standard interscalene block. Sixty adults having shoulder surgery will receive one of the two blocks before their operation. Researchers will measure how quickly hand grip strength returns and how well pain is controlled afterward.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- local anesthetic (e.g., bupivacaine)
- What this could lead to
- If PENG block works as well for pain but spares muscle strength, patients could recover hand and arm function faster after shoulder surgery.
- What could go wrong
- This is a small, early-stage study with only 60 participants. The PENG block may not provide enough pain relief, or the muscle-sparing benefit may be minimal.
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
-
60 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Dec 2025
- 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
-
22 to 60 years
- Sex
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Anyone
- Healthy volunteers
-
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: * Adult patients of the specified age range * Any gender * American Society of Anaesthesiologists physical status grades 1 and 2 * Body mass index less than 35 * Duration of surgery between 90 to 120 minutes Exclusion Criteria: * American Society of Anaesthesiologists physical status grades 3 and 4 * Allergy to local anesthetics * Coagulation disorder (INR \>1.2, Platelets \<100,000), or recent intake of clopidogrel or warfarin within 1 week * Active infection at site of injection
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Cairo University
Cairo, 11562, Egypt
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