← Eichor
Study identifier: NCT06942689 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Determination of the Optimal Volume of Liposomal Bupivacaine in Adductor Canal Block for Knee Joint Surgery

Condition: Optimal Volume of Liposomal Bupivacaine  ·  Sponsor: Nanjing First Hospital, Nanjing Medical University

PhasePhase 4
Planned participants63
Who can joinAll sexes, 18 Years to 85 Years
Healthy volunteersNo

About this study

Building on Bayesian design methodologies from volume optimization studies of ropivacaine in shoulder surgery, this study pioneers the application of a seamless dose-finding strategy in knee ACB. Utilizing advanced statistical models (BOIN/BOP2 design), we aim to systematically evaluate the volume-effect relationship of liposomal bupivacaine, providing precise dosing recommendations to advance personalized and optimized analgesic protocols for knee surgery.

This description comes directly from the study's public registry record.

Talk to the study team

Liu Han  ·  18951670163  ·  han_cold.student@sina.com

Always discuss trial participation with your own doctor first.

Locations (1)

Nanjing First HospitalNanjing, Jiangsu, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06942689