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Efficacy and Safety of Anrikefon Injection for Multimodal Postoperative Analgesia in Patients Undergoing Laparoscopic Hepatectomy

StatusNot Yet Recruiting
PhasePhase 4
Started2026-08-30
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A single-center, randomized, double-blind, placebo-controlled trial design will be adopted to investigate whether Anruikefon can significantly reduce the consumption of sufentanil via PCIA pumps within 48 hours postoperatively compared with placebo.
Trial Details
NCT Number NCT07801183
Lead Sponsor Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Conditions Postoperative Acute Pain
Enrollment 117 participants
Start Date 2026-08-30
Primary Completion 2027-07-01 (estimated)
Study Completion 2027-07-30 (estimated)
Updated on ClinicalTrials.gov 2026-09-03