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The effects of ultrasound-guided infraspinatus fascia block and brachial plexus superior trunk block on postoperative pain and recovery quality in patients undergoing shoulder arthroscopy surgery

The effects of ultrasound-guided infraspinatus fascia block and brachial plexus superior trunk block on postoperative pain and recovery quality in patients undergoing shoulder arthroscopy surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087072
Enrollment
Unknown
Registered
2024-07-19
Start date
2024-07-24
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Postoperative pain and recovery quality of patients undergoing shoulder arthroscopy surgery

Interventions

Intervention group:30 minutes before induction, 15ml of 0.375% ropivacaine was used for ultrasound-guided brachial plexus block. Conventional general anesthesia induction was performed, and a combinat
Control group:30 minutes before induction, 30ml of 0.375% ropivacaine was used for ultrasound-guided infraspinatus teres muscle fascial block. Conventional general anesthesia induction was performed,

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients planning to undergo elective shoulder arthroscopic surgery; (2) Age range: 18-65 years old

Exclusion criteria

Exclusion criteria: (1) Previous presence of obstructive or restrictive pulmonary disease; (2)BMI >35kg/m2; (3) Coagulation dysfunction; (4) Liver or kidney failure; (5) Pregnancy; (6) Allergy to local anesthetics; (7) Chronic opioid use; (8) Previous neck or supraclavicular surgeries; (9) Pre-existing neurological defects or neuropathy affecting the brachial plexus; (10) Patients with ASA grade IV or higher; (11) Patients undergoing revision, flushing, and debridement surgeries; (12)Poor control of hypertension;

Design outcomes

Primary

MeasureTime frame
Worst resting pain score within 24 hours after surgery(NRS,0-10));

Secondary

MeasureTime frame
Restore quality rating;Incidence of diaphragmatic paralysis;Area under the pain score curve 24 hours after surgery;The dosage of analgesic drugs used;Postoperative nausea and vomiting;Blocking complications;Duration of analgesia;Diaphragmatic mobility ;Hospitalization satisfaction score;

Countries

China

Contacts

Public ContactYan Ming

The Affiliated Hospital of Xuzhou Medical University

yjy3001@163.com+86 180 5226 8329

Outcome results

None listed

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