drugset / Trial / NCT07606911

Effect of Liposomal Bupivacaine on Rebound Pain After Peripheral Nerve Block in Orthopedic Surgery.

NCT07606911

RandomizedParallel-groupTriple-blindPrevention

Summary

This study will prospectively compare the preventive effect of liposomal bupivacaine combined with plain bupivacaine versus plain bupivacaine alone on rebound pain after nerve block in patients undergoing orthopedic extremity surgery. The primary aim is to assess whether the combination reduces the incidence or severity of rebound pain (i.e., more effectively covers the postoperative inflammatory peak on days 2-3 and provides a smoother regression curve of sensory blockade). Secondary aims include evaluation of upper limb functional scores, occurrence of chronic pain, and health-related quality of life. All aims will be assessed over 72 hours or the duration of hospitalization if shorter.

Timeline

Start
2026-07-01
Primary completion
2027-07-01
Completion
2027-12-01

Drugs

EvaluationDrugModalityDoseRoute
Background Bupivacaine Other / unclassified 133 mg
Background Bupivacaine Other / unclassified 75 mg

Indications

No indication recorded.