Clinical trial · Interventional
Erector Spinae Versus Intercostal Nerve Blocks With Liposomal Bupivacaine for Analgesia in Thoracic Surgery
NCT06810375CI-TRIAL-00107779recruitingPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This clinical trial compares efficacy in postoperative pain management in thoracic surgery between erector spinae block versus liposomal bupivacaine injections.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancers | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Erector Spinae (ESP) Block with Bupivacaine (Marcaine®) | Drug | — | UNRESOLVED |
| Intercostal nerve block | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Preoperative Erector Spinae Block (ESB)(Bupivacaine)(Marcaine®)
- interventionNames
- Drug: Erector Spinae (ESP) Block with Bupivacaine (Marcaine®)
- Drug: Intercostal nerve block
- type
- ACTIVE_COMPARATOR
- label
- Intraoperative Intercostal Nerve Block (INB)(Liposomal Bupivacaine)(Exparel®)
- interventionNames
- Drug: Erector Spinae (ESP) Block with Bupivacaine (Marcaine®)
- Drug: Intercostal nerve block
Primary outcomes (2)
- measure
- Postoperative pain control assessment
- timeFrame
- Up to 48 hours postoperatively
- description
- Study team will assess postoperative pain scores at 6, 12, 24 and 48 hours (Minimum numerical pain score of 0 and a maximum of 10)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 90 Years
Show eligibility criteria text
Inclusion Criteria: * Video assisted pulmonary resection, pleurodesis or decortication Exclusion Criteria: * Allergy to local anesthetics * Patient undergoing bilateral surgery * Surgery is emergent as deemed by the principal investigator
References
Publications (0)
Data not yet available
No reference posted for this study.