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Liposomal bupivacaine plus bupivacaine hydrochloride versus bupivacaine hydrochloride alone for post-craniotomy scalp nerve block analgesia

ChiCTR2600133590Phase 4Not yet recruiting

Sponsor
Peking University Shenzhen Hospital
Start
Oct 2026
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Countries
1
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Overview

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.

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Drugs

liposomal bupivacainebupivacaine
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Conditions

Post-craniotomy pain

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