Clinical Trial

Anrikefon-based Patient-controlled Intravenous Analgesia After Laparoscopic Surgery

Terminated Phase 4
View on ClinicalTrials.gov →
Why the trial stopped
The study was terminated due to substantial protocol amendments involving changes in the target population and primary endpoint, rendering previously collected data incompatible with the revised study objective.
Summary
Visceral pain following laparoscopic surgery is frequently underestimated, yet it is associated with a range of adverse outcomes. Effective visceral pain management should constitute an essential component of postoperative analgesic strategies following laparoscopic procedures. However, conventional analgesic agents, including μ-opioid receptor agonists, lack specificity for visceral pain. Anrikefon, a novel selective peripheral κ-opioid receptor agonist, demonstrates unique efficacy in alleviating visceral pain with a favorable safety profile. Preliminary studies showed that a single intravenous dose of anrikefon effectively alleviates postoperative pain after abdominal surgery with a low risk of adverse effects. The investigators hypothesize that an appropriate dosing regimen of anrikefon administered via patient-controlled intravenous analgesia (PCIA) pump, as part of a multimodal analgesic strategy, can specifically target and alleviate visceral pain after laparoscopic surgery, thereby achieving comprehensive postoperative analgesia.
Protocol Amendment History 4 changes
critical Trial terminated 2026-04-10
notable Enrollment reduced: 140 -> 13 participants 2026-04-10
notable Primary completion moved earlier: 2026-10 -> 2026-02-11 2026-04-10
minor Completion moved earlier: 2026-11 -> 2026-03-11 2026-04-10
Trial Details
NCT Number NCT07246785
Lead Sponsor Peking University First Hospital
Conditions Laparoscopic Surgery, Visceral Pain, Postoperative, Anrikefon, Patient-controlled Intravenous Analgesia
Enrollment 13 participants
Start Date 2025-12-25
Primary Completion 2026-02-11 (estimated)
Study Completion 2026-03-11 (estimated)
Updated on ClinicalTrials.gov 2026-04-09