Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
ChiCTR2600124270Phase 4Not yet recruiting
Phase 4, randomised, double-blind trial in postoperative pain comparing Experimental group: bupivacaine + liposomal bupivacaine with Control group: bupivacaine monotherapy (2 arms). Primary endpoint: Area under NRS score curve (AUC) at rest 12–72 hours postoperatively. Planned start May 2026; status: not yet recruiting.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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