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Comparison of modified upper trunk block and traditional intermuscular groove block with bupivacaine liposomes in analgesia after shoulder arthroscopy

Comparison of modified upper trunk block and traditional intermuscular groove block with bupivacaine liposomes in analgesia after shoulder arthroscopy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076523
Enrollment
Unknown
Registered
2023-10-11
Start date
2023-10-11
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rotator cuff injury

Interventions

ISTB group:Bupivacaine liposomes 2.5ml+0.5% levobupivacaine 2.5ml will be injected between the three branches of the upper trunk
ISB group:Bupivacaine liposome 7.5ml +0.5% levobupivacaine 7.5ml will be injected between the C5 and C6 nerve roots

Sponsors

the Second Affiliated Hospital & Yuying Children's Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.eletive arthroscopic rotator cuff repair of shoulder 2.18-65 years old 3.American Society of Anesthesiologists (ASA) Grade I or II

Exclusion criteria

Exclusion criteria: Cannot sign informed consent for this study; Communication barriers; Combined with severe obstructive or restrictive lung disease; Body Mass Index (BMI) >35 kg/m2; Coagulation disorders; Liver or kidney failure; Be pregnant; Local anesthetic allergy; History of chronic opioid use (such as morphine hydrochloride sustained-release tablets, oxycodone hydrochloride sustained-release tablets, fentanyl transdermal patches, etc.); Surgical history of neck or supraclavicular fossa on the operative side; Sensory and motor disorders of the upper extremity on the operative side; Large rotator cuff tear (tear > 5 cm; Involved 2 or more tendon tears)

Design outcomes

Primary

MeasureTime frame
24h post-operative resting NRS pain score;The incidence of hemidiaphragm paralysis;

Secondary

MeasureTime frame
Resting pain score and opioid consumption at each observation time point;Changes in pulmonary function and pulse oxygen saturation;Sensory and motor block duration;Satisfaction with analgesia;Adverse reactions and neurological complications;

Countries

China

Contacts

Public ContactWu Hong

the Second Affiliated Hospital & Yuying Children's Hospital, Wenzhou Medical University

redaspirin@163.com+86 182 6785 6135

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026