drugset / Trial / NCT07171125

Liposomal Bupivacaine for Pain After Lumbar Fusion

NCT07171125 ↗

Phase 4 Completed 204 enrolled Min Li
RandomizedParallel-groupDouble-blindTreatment

Summary

Spine surgery often causes severe postoperative pain. Currently, our hospital routinely uses ropivacaine for local infiltration analgesia (lasting 6-8 hours). This study evaluates liposomal bupivacaine, a novel long-acting local anesthetic providing up to 72 hours of pain relief, in patients undergoing posterior lumbar spine surgery. Through a randomized controlled design, we will compare the two drugs' effects on pain control within 72 hours and opioid consumption. Both regimens are guideline-recommended and safe.

Timeline

Start
2025-09-20
Primary completion
2026-02-28
Completion
2026-03-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 25 mg Other
Subject Bupivacaine Other / unclassified 266 mg Other
Comparator Ropivacaine Other / unclassified 120 mg Other