Anrikefon-based Patient-controlled Intravenous Analgesia Following Laparoscopic Surgery

Recruiting Phase 4 Interventional Study
Laparoscopic Surgery Visceral Pain, Postoperative Anrikefon Patient-controlled Intravenous Analgesia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 75
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
140 (estimated)
Sponsor
Peking University First Hospital · Other
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About This Trial
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. Anrikef…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Aged \>= 18 years but \< 75 years; 2. Scheduled to undergo elective laparoscopic colorectal surgery with an expected duration of \>=1 hour; 3. The incisional pain can be covered by the transversus abdominis plane block or rectus sheath block; yet patients still require postop…
Contacts

Dong-Xin Wang, MD, PhD

8610 83572784

wangdongxin@hotmail.com

CONTACT

Chun-Qing Li, MD

8610 83575138

lichuntsing@163.com

CONTACT