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The effect of ultrasound-guided anterior fascial external suprascapular nerve block combined with axillary nerve block on postoperative pain relief and phrenic nerve function in shoulder arthroscopic surgery: a descriptive study

The effect of anterior vertebral fascia external suprascapular nerve block combined with axillary nerve block on postoperative pain relief and phrenic nerve function in shoulder arthroscopic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083270
Enrollment
Unknown
Registered
2024-04-19
Start date
2024-04-22
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Shoulder joint injury

Interventions

Neuroblock group:Combination of suprascapular nerve and axillary nerve block

Sponsors

Beijing Friendship Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: A. Planned to undergo elective shoulder arthroscopic surgery under general anesthesia; B. Age range from 18 to 70 years old; C. BMI 18-30 kg/m2; D. ASA grade I to III; E. Understand the contents of the informed consent form and agree to sign the informed consent form before this study.

Exclusion criteria

Exclusion criteria: A. There are contraindications for regional nerve block (puncture site infection, coagulation dysfunction, local anesthetic allergy); B. Concomitant chronic pulmonary and bronchial diseases, old cerebral infarction, transient ischemic attacks, sleep apnea syndrome, liver and kidney dysfunction, or mental illness; C. Huge shoulder sleeve tear; D. Long term use of opioid drugs; E. Transitioning from surgery to open surgery; F. Refusing to sign informed consent forms, etc

Design outcomes

Primary

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

Secondary

MeasureTime frame
Sensory blockade effect 10 minutes after blockade;Resting NRS scores at 1 hour, 6 hours, 12 hours, and 24 hours after surgery;Time of first use of opioid drugs;Times of Rescue analgesia;The incidence of diaphragmatic paralysis after 10 minutes of block and PACU;Adverse event occurrence rate;Patient satisfaction;Blocking success rate;Dosage of remifentanil during surgery;Postoperative complications (such as postoperative nausea and vomiting, skin itching, respiratory depression<10 beats/minute, and excessive sedation related to opioid drug use; block related complications such as pneumothorax, hematoma, infection, intestinal perforation, and local anesthetic poisoning; surgical complications within 24 hours after surgery such as severe arrhythmia, heart failure, acute myocardial infarction, respiratory failure, pulmonary infection, pulmonary embolism, and stroke;

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