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Effect of ultrasound-guided C5-6 nerve root block versus conventional scalene intermuscular groove brachial plexus block on ipsilateral shoulder pain and lung function after thoracic surgery: a randomized controlled trial

Effect of ultrasound-guided C5-6 nerve root block versus conventional scalene intermuscular groove brachial plexus block on ipsilateral shoulder pain and lung function after thoracic surgery: a randomized controlled trial

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082939
Enrollment
Unknown
Registered
2024-04-11
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Lung tumor

Interventions

Group A (Interscalene brachial plexus block group):Interscalene brachial plexus block
Group B (C5-6 nerve root block group):C5-6 nerve root block

Sponsors

The First Affiliated Hospital of Kunming Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients undergoing selective lobectomy and segmental resection under general anesthesia; (2) Age 18-70 years old; (3) ASA classification I-III; (4) BMI 18 ~ 28kg/?; (5) Patients and their families agreed and signed the anesthesia consent before operation (6) There is no serious language communication obstacle, and the postoperative follow-up content can be agreed and accepted after explanation;

Exclusion criteria

Exclusion criteria: (1) Patients with severe heart, lung, brain, liver and kidney dysfunction and severe endocrine system diseases; (2) Patients with COPD, asthma, pulmonary fibrosis and other basic lung disease history before surgery; (3) Nonoperative phrenic nerve paralysis; (4)Patients undergoing emergency surgery or conversion to thoracotomy; (5)Patients who may be allergic to the study drug or have an infection at the injection site; (6) Patients with coagulation dysfunction or long-term anticoagulation before operation; (7) Patients with a history of shoulder disease or surgery for shoulder trauma; (8) Patients with long-term antidepressant or psychotropic drug use or alcoholism; (9) Patients with mental illness or communication disorder or refusing to cooperate;(10) Ultrasonic coupling agent allergy.

Design outcomes

Primary

MeasureTime frame
Ipsilateral shoulder pain score(NRS) 48 hours after surgery;

Secondary

MeasureTime frame
Postoperative diaphragmatic paralysis;Changes in lung function;Postoperative pulmonary complications;

Countries

China

Contacts

Public ContactYu Fang

The First Affiliated Hospital of Kunming Medical University

fangyu@ydyy.cn+86 138 8809 1314

Outcome results

None listed

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