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Comparison of analgesic efficacy and safety of ultrasound-guided thoracic paravertebral block combined with erector spinae or serratus anterior block in minimally invasive thoracic surgery

Comparison of analgesic efficacy and safety of ultrasound-guided thoracic paravertebral block combined with erector spinae or serratus anterior block in minimally invasive thoracic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200063686
Enrollment
Unknown
Registered
2022-09-14
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Minimally invasive postoperative analgesia in thoracic surgery

Interventions

thoracic paravertebral block combined with erector spinae or serratus anterior block :none

Sponsors

Zhongda Hospital, School of Medicine, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18-75 years who underwent elective thoracoscopic minimally invasive surgery; ASA grade I ~III; BMI is 18 ~ 30 kg/m2; Successfully completed the operation and wake up.

Exclusion criteria

Exclusion criteria: Coagulation dysfunction, infection and ulceration of puncture site; Allergic to local anesthetics or opioids; Regional block was refused; Patients with a history of general anesthesia within 6 months before surgery; Chronic pain, history of mental illness; History of drug and alcohol abuse; Serious cardiovascular and cerebrovascular diseases, liver and kidney dysfunction; Chronic bronchitis, COPD disease history; Abnormal lung function, maximum volume of gas (MVV) 50% lower than the expected value, forced expiratory volume in 1 second (PEV1) 50% lower than the expected value; Conversion to thoracotomy or severe postoperative complications resulted in prolonged hospital stay.

Design outcomes

Primary

MeasureTime frame
Total analgesic drug consumption within 24 hours after operation;Pain scores;Analgesic Remedy Situation;

Secondary

MeasureTime frame
The occurrence of adverse reactions;

Countries

China

Contacts

Public ContactMeng-Meng Zheng

Zhongda Hospital, School of Medicine, Southeast University

zmm9474@163.com13813289474

Outcome results

None listed

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