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Randomized controlled study of modified upper trunk block and interscalene brachial plexus block for analgesia of arthroscopic shoulder surgery

Randomized controlled study of modified upper trunk block and interscalene brachial plexus block for analgesia of arthroscopic shoulder surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031178
Enrollment
Unknown
Registered
2020-03-23
Start date
2020-03-25
Completion date
Unknown
Last updated
2020-05-04

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

Conditions

Postoperative Pain

Interventions

Group 1:the modified upper trunk block
Group 2:the interscalene brachial plexus block

Sponsors

Department of Anesthesiology, Beijing Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged more than 18 years and less than 80 years; 2. American Society of Anesthesiologists physical status I to III; 3. Scheduel for shoulder joint arthroscopic surgery; 4. Patients who can sign the informed consent of this study;

Exclusion criteria

Exclusion criteria: 1. Patients with severe obstructive or restrictive pulmonary disease; 2. BMI>35kg/m2; 3. Patients with coagulation disorders; 4. Patients with liver or kidney failure; 5. Pregnant patients; 6. Patients with local anesthetic allergy; 7. Patients using chronic opioids; 8. Patients with surgical history of the neck or supraclavicular region on the operative side; 9. Patients with sensory and motor disorders of the upper limb on the operative side; 10. Patients undergoing shoulder arthroscopic revision, lavage and debridement.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale pain scores at rest at 30min in postanesthesia care unit after arthroscopic shoulder surgery;

Secondary

MeasureTime frame
Numeric Rating Scale pain scores at rest at other time points after surgery;Cumulative morphine consumption at 24h after surgery;Diaphragmatic excursions;Pulmonary function;Grip strength;Block duration;pulse oxygen saturation;patient satisfaction with pain relief;Incidence of adverse effects;

Countries

China

Contacts

Public ContactHongye Zhang

Department of Anesthesiology, Beijing Hospital

anaesthesia119@163.com+86 861085136404

Outcome results

None listed

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