External Oblique Intercostal Plane Block for Postoperative Analgesia After Major Upper Abdominal Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorJun Zhang

About this trial

Postoperative pain after laparoscopic major upper abdominal surgery (e.g., gastric, hepatic, gallbladder, pancreatic surgery) is often severe, and inadequate analgesia may lead to increased opioid use, opioid dependence, and poor functional recovery. Current analgesic techniques such as neuraxial block have safety concerns (e.g., hypotension, neurological injury), while transversus abdominis plane (TAP) block is ineffective for blocking the lateral cutaneous branches of intercostal nerves in the upper abdomen. The External Oblique Intercostal Plane Block (EOIB) is a novel regional block technique that has shown promise in reducing postoperative opioids and pain in small-scale studies, but evidence for its use in major upper abdominal surgery is limited. This randomized controlled trial (RCT) aims to evaluate the analgesic efficacy and safety of bilateral EOIB combined with standard multimodal analgesia versus standard multimodal analgesia alone in patients undergoing elective laparoscopic major upper abdominal surgery. The primary outcome is the total postoperative opioid consumption (measured as Morphine Milligram Equivalents, MME) within 24 hours. Secondary and additional outcomes include pain scores (Verbal Rating Scale, VRS), recovery quality (QoR-15 scale), incidence of adverse events, and hospital stay.

Eligibility criteria

Qualifiers

Obtain written informed consent from participants or their legal representatives

Age between 18 and 85 years

American Society of Anesthesiologists (ASA) physical status classification I-III

Scheduled for elective laparoscopic major upper abdominal surgery (e.g., gastric, hepatic, gallbladder, pancreatic surgery)

Disqualifiers

Hepatic disease (liver enzyme levels ≥ 2× the upper limit of normal)

Renal disease (serum creatinine levels ≥ 2× the upper limit of normal)

Allergy to local anesthetics or known study-related drugs

Pregnancy or lactation

Trial design

Treatments tested in this trial

  • External Oblique Intercostal Plane Block
  • Standard multimodal analgesia

Treatment groups

78 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Jun Zhang

Lead sponsor

Fudan University

Sponsor institution