Clinical Trial

Liposomal Bupivacaine Versus Ropivacaine for Preperitoneal Infiltration Analgesia in Upper Abdominal Laparotomy

Completed
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Summary
Upper abdominal open surgery is associated with significant trauma, and postoperative pain management poses considerable challenges. The inflammatory response triggered by peritoneal incision and the transmission of visceral pain via the vagus nerve are key components of "surgical stress" and pain. A potential intervention strategy involves the local administration of anesthetic agents to suppress peritoneal overreaction and block the cascade of pro-inflammatory cytokines in related nerves. Liposomal bupivacaine, as a long-acting local anesthetic, may provide more prolonged postoperative analgesia compared to ropivacaine. Therefore, this trial aims to prospectively compare the analgesic efficacy and anti-inflammatory effects of the two drugs when administered as pre-closure preperitoneal infiltration. Secondary endpoints include opioid consumption, complication rates, and postoperative recovery indicators, to comprehensively evaluate their clinical value.
Protocol Amendment History 1 change
critical Trial completed 2026-07-16
Trial Details
NCT Number NCT07271979
Lead Sponsor Qilu Hospital of Shandong University
Conditions Liposomal Bupivacaine, Preperitoneal Infiltration, Analgesia
Enrollment 146 participants
Start Date 2026-01-04
Primary Completion 2026-04-23 (estimated)
Study Completion 2026-05-23 (estimated)
Updated on ClinicalTrials.gov 2026-07-15