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Study identifier: NCT07525986 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Anrikefon-based Patient-controlled Intravenous Analgesia Following Laparoscopic Surgery

Condition: Laparoscopic Surgery · Visceral Pain, Postoperative · Anrikefon  ·  Sponsor: Peking University First Hospital

PhasePhase 4
Planned participants140
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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.

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

Talk to the study team

Dong-Xin Wang, MD, PhD  ·  8610 83572784  ·  wangdongxin@hotmail.com

Chun-Qing Li, MD  ·  8610 83575138  ·  lichuntsing@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Peking University First HospitalBeijing, Beijing Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07525986