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Comparison of subclavian brachial plexus combined with anterior suprascapular nerve block and brachial plexus superior trunk block for postoperative analgesia in shoulder arthroscopic surgery: a randomized controlled non-inferiority study

Comparison of subclavian brachial plexus combined with anterior suprascapular nerve block and brachial plexus superior trunk block for postoperative analgesia in shoulder arthroscopic surgery: a randomized controlled non-inferiority study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080933
Enrollment
Unknown
Registered
2024-02-18
Start date
2024-02-19
Completion date
Unknown
Last updated
2024-02-19

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

Conditions

Shoulder joint disease, shoulder joint injury, rotator cuff injury

Interventions

Superior trunk block group (Group B):Brachial plexus superior trunk block
Anterior combined block group (Group S):Combined block of subclavian brachial plexus and anterior suprascapular nerve

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Planned elective surgery under general anesthesia 2: Age 18-70 years old 3: BMI18-30 kg /m2 4: ASA grade 1 to 3 5: Understand the informed consent form and agree to sign the informed consent form before this study

Exclusion criteria

Exclusion criteria: 1.There are contraindications for regional nerve block (puncture site infection, coagulation dysfunction, local anesthetic allergy) 2.Concomitant chronic pulmonary and bronchial disease, old cerebral infarction, transient ischemic attack, sleep apnea syndrome, liver and kidney dysfunction, or mental illness 3.Severe rotator cuff tear 4.frequently use of opioid drugs 5.Transition from minimally invasive surgery to open surgery 6.Refusal to sign informed consent form

Design outcomes

Primary

MeasureTime frame
Opioid dosage for the first 24 hours after surgery;

Secondary

MeasureTime frame
Sensory and motor block effects;Resting NRS score;The incidence of diaphragmatic paralysis;Time of the first analgesia;Times of analgesia;Postoperative complications;Patient satisfaction;The success rate of block;Intraoperative dosage of remifentanil;Hospitalization days;24-hour postoperative QoR-15 score;

Countries

China

Contacts

Public ContactHu zhenfa

Beijing Friendship Hospital, Capital Medical University

huzhenfa1008@sina.com+86 159 0154 7614

Outcome results

None listed

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