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Analysis of the efficacy and safety of liposomal bupivacaine for erector spinae plane block in thoracoscopic surgery

Analysis of the efficacy and safety of liposomal bupivacaine for erector spinae plane block in thoracoscopic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113344
Enrollment
Unknown
Registered
2025-11-27
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

lung cancer

Interventions

Sponsors

The First Affiliated Hospital of Nanchang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Before the trial, understand the nature, significance, possible benefits, possible inconveniences and potential dangers of the trial, understand the study procedures, and voluntarily sign the informed consent form. 2. Patients who underwent thoracoscopic lobectomy with the same group of doctors; 3. Male or female, age 18-65 years old; 4. Male weight >= 50kg, female weight =45kg, BMI 19.0~26.0kg/m^2; 5. Anesthesia ASA rating is II~II.

Exclusion criteria

Exclusion criteria: 1. Patients refuse erector spinae block; 2. Patient has a previous specific allergic disease (asthma, urticaria, eczema, etc.) or known allergy to bupivacaine; 3. Patients with severe liver and kidney dysfunction; 4. The patient has a previous history of chronic neuropathic pain.

Design outcomes

Primary

MeasureTime frame
Cumulative value of NRS pain score;

Secondary

MeasureTime frame
Nerve block plane;Postoperative analgesic drug dose;Endotracheal intubation removal time;Time of drain remova;Sufentanil and remifentanil dosage;ICU stay time;

Countries

China

Contacts

Public ContactYang Zhang

The First Affiliated Hospital of Nanchang University

mzzhangyang@126.com+86 13576080494

Outcome results

None listed

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