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Impact of Bupivicaine Liposome Intercostal Nerve Block versus PCIA on the Incidence of chronic post-surgery pain in thoracic surgery patients: A Single-Center, Observational, Cohort Study

Impact of Bupivicaine Liposome Intercostal Nerve Block versus PCIA on the Incidence of chronic post-surgery pain in thoracic surgery patients: A Single-Center, Observational, Cohort Study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600120261
Enrollment
Unknown
Registered
2026-03-11
Start date
2025-10-22
Completion date
Unknown
Last updated
2026-03-16

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

Conditions

Chronic Post-surgery Pain

Interventions

Intraoperative Intercostal Nerve Block with Liposomal Bupivacaine Group:None
Postoperative PCIA Analgesia Group:None

Sponsors

Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-75 years old ; 2. Undergoing elective uniportal video-assisted thoracoscopic surgery (VATS) for pulmonary surgery; 3. Receiving intraoperative intercostal nerve block with liposomal bupivacaine or postoperative patient-controlled intravenous analgesia (PCIA); 4. ASA classification of ?- ?.

Exclusion criteria

Exclusion criteria: 1. Patients whose surgical approach was altered during the procedure for any reason (e.g., conversion to thoracotomy); 2. Patients requiring invasive clinical interventions (e.g., thoracentesis) due to postoperative complications (e.g., pneumothorax); 3. Patients with preoperative analgesic dependence; 4. Patients with a history of chronic pain prior to surgery; 5. Patients undergoing reoperation within 3 months post-surgery; 6. Patients experiencing severe adverse events postoperatively, such as severe allergic reactions or mortality; 7. Patients with missing relevant clinical data; 8. Patients lost to follow-up within 3 months after surgery.

Design outcomes

Primary

MeasureTime frame
The incidence of Chronic Post-surgery Pain at 3 months after surgery.;The degree of Chronic Post-surgery Pain at 3 months after operation.;The nature of Chronic Post-surgery Pain at 3 months after operation;

Secondary

MeasureTime frame
Incidence of postoperative use of additional analgesics;NRS score at 24 and 72 hours after surgery;Incidence of adverse events within 24 and 72 hours postoperatively;The incidence of complication after surgery;the length of stay;the general expenses during hospitalization;The incidence of skin numbness in the operation area at 3 months after surgery;12-Item Short-Form Health Survey (SF-12) score at 3 months postoperatively;Time to first use of additional analgesic medication postoperatively;Types of rescue analgesia used postoperatively;

Countries

China

Contacts

Public ContactXiaohua Zou

Affiliated Hospital of Guizhou Medical University

562931613@qq.com+86 138 0941 6036

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 20, 2026