Clinical study on analgesic effect of anterior serratus block combined with ice compress after thoracoscopic pneumonectomy

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100050539

Enrollment

Unknown

Registered

2021-08-28

Start date

2021-10-01

Completion date

Unknown

Last updated

2022-05-02

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

Conditions

Pain after lung surgery

Interventions

Control group:conventional analgesic pump

Experimental group1:Preoperative ultrasound-guided serratus anterior block and postoperative analgesia pump analgesia

Experimental group2:Postoperative ice compress for 24 hours and analgesic pump for analgesia

Experimental group3:Preoperative ultrasound-guided serratus anterior block combined with postoperative ice compress for 24 hours and postoperative analgesia pump analgesia

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Endoscopic thoracic pneumonectomy, including bullae resection, lung wedge resection, segmentectomy, and radical resection of lung cancer 2. BMI 1825kg/m2; 3. Agree to accept this analgesic program; 4. Voluntary participation in this research.

Exclusion criteria

Exclusion criteria: 1. Sensitive to cold; 2. History of lung surgery; 3. History of opioid or alcohol abuse; 4. History of chronic pain; 5. History of Raynaud's disease.

Design outcomes

Primary

Measure	Time frame
Athens Insomnia Scale;	—

Secondary

Measure	Time frame
C-reactive protein;White blood cell count;	—

Countries

China

Contacts

Public ContactXu Zhipeng

Affiliated Hospital of Jiangsu University

xu630371236@163.com+86 15262921001

Outcome results

None listed

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