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Study identifier: NCT07474896 Synced from ClinicalTrials.gov · July 29, 2026
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Diaphragm-Sparing Regional Anesthesia Techniques for Shoulder Surgery

Condition: Osteoarthritis Shoulder  ·  Sponsor: Poznan University of Medical Sciences

PhaseNA
Planned participants70
Who can joinAll sexes, 65 Years to 100 Years
Healthy volunteersNo

About this study

This study will compare two regional anesthesia techniques for shoulder surgery and evaluate their effects on diaphragmatic function. The standard regional anesthesia technique for shoulder surgery is the interscalene brachial plexus block (ISB), which provides effective analgesia but is frequently associated with ipsilateral hemidiaphragmatic paresis due to phrenic nerve involvement. An alternative diaphragm-sparing strategy is the combination of a suprascapular nerve block (SSNB) and an infraclavicular brachial plexus block (ICB), which may reduce the risk of diaphragmatic dysfunction while maintaining effective analgesia for shoulder surgery. All participants will receive ultrasound-guided regional anesthesia prior to surgery and will be randomly assigned to one of two groups: Group 1: Interscalene brachial plexus block Group 2: Suprascapular nerve block combined with infraclavicular brachial plexus block The primary aim of this study is to determine whether the diaphragm-sparing technique reduces the incidence of hemidiaphragmatic paresis while providing analgesia comparable to the standard interscalene block. Diaphragmatic movement will be assessed using ultrasound before and after block placement. Secondary outcomes include postoperative pain intensity, opioid consumption, pulmonary function parameters, and block-related complications.

This description comes directly from the study's public registry record.

Talk to the study team

Malgorzata Reysner, MD PhD  ·  +48618738313  ·  mreysner@ump.edu.pl

Always discuss trial participation with your own doctor first.

Locations (1)

Poznan University of Medical SciencesPoznan, PolandRecruiting

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Source record: clinicaltrials.gov/study/NCT07474896