drugset / Trial / NCT07366905

Clinical Observation of Bupivacaine Liposome for Lower Extremity Nerve Block

NCT07366905

NaSequentialOpen-labelHealth-services research

Summary

This prospective, sequential dose-finding clinical observational study aims to estimate the median effective concentration (EC50) and the 95% effective concentration (EC95) of liposomal bupivacaine for ultrasound-guided femoral nerve block. Sensory and motor block endpoints are evaluated separately at 30 minutes after block placement using a modified up-and-down (sequential allocation) design, with trial termination after eight reversal points.

Timeline

Start
2026-02-01
Primary completion
2026-03-31
Completion
2026-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Bupivacaine Other / unclassified 266 mg

Indications

No indication recorded.