Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
ChiCTR2600133590Phase 4Not yet recruiting
Phase 4, randomised trial in Post-craniotomy pain comparing Bupivacaine hydrochloride group with Liposomal bupivacaine plus bupivacaine hydrochloride group (2 arms). Primary endpoint: Area under the curve of resting numerical rating scale pain scores from 12 to 72 hours after completion of the scalp nerve block. Planned start Oct 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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