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Effect of ultrasound-guided costoclavicular versus interscalene block with propofol sedation for arthroscopic shoulder surgery: a randomized, prospective, non-inferiority study

Effect of ultrasound-guided costoclavicular versus interscalene block with propofol sedation for arthroscopic shoulder surgery: a randomized, prospective, non-inferiority study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040841
Enrollment
Unknown
Registered
2020-12-11
Start date
2020-12-14
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Arthroscopic shoulder surgery

Interventions

Costoclavicular group:Costoclavicular block
Interscalene group:Interscalene block

Sponsors

Guangzhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 232 patients of American Society of Anesthesiologists (ASA) physical status I to III patients, aged 18 to 75 years, presented for surgery of the arthroscopic shoulder surgery were enrolled in this study.

Exclusion criteria

Exclusion criteria: Patient refused; Coagulopathy; Hypersensitivity to local anesthetics; Localised infection; Severe liver and kidney dysfunction; Severe pulmonary dysfunction; Mental illness; History of drug abuse; body mass index more than 35kg/m2.

Design outcomes

Primary

MeasureTime frame
Motor block;Diaphragmatic paralysis;—

Secondary

MeasureTime frame
Sensory block;Operation related adverse events;Anesthesia related indicators;Surgical related indicators;postoperative analgesia related indicators;—

Countries

China

Contacts

Public ContactZheng Junyi
dswzheng@163.com+86 13763377393

Outcome results

None listed

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