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临床试验/NCT07082387
NCT07082387已完成不适用

External Oblique and Rectus Abdominis Plane (EXORA) Block Versus Quadratus Lumborum Block for Postoperative Analgesia in Patients Undergoing Laparoscopic Cholecystectomy

Tanta University1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年7月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
80
试验地点
1
主要终点
Time to the 1st rescue analgesia

研究概览

简要总结

This study aims to compare the effects of the external oblique and rectus abdominis plane (EXORA) block and the quadratus lumborum block (QLB) on postoperative analgesia in patients undergoing laparoscopic cholecystectomy (LC).

详细描述

Laparoscopic cholecystectomy (LC) is a proven, gold standard surgical procedure for the management of gallbladder stones.

The quadratus lumborum block (QLB) is a regional block that would appear to be similar to the posterior TAP block, although the drug injection area is deeper and more dorsal than the transverse abdominal aponeurosis.

The external oblique and rectus abdominis plane (EXORA) block is an emerging technique providing a sensory block to the anterolateral abdominal wall.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age from 18 to 65 years.
  • •Both sexes.
  • •American Society of Anesthesiology (ASA) physical status I-II.
  • •Undergoing laparoscopic cholecystectomy (LC) under general anesthesia.

排除标准

  • •History of allergies to local anesthetics.
  • •Opioid dependency.
  • •Bleeding or coagulation disorders.
  • •Psychiatric and neurological disorder.
  • •Local infection at the site of injection.
  • •Body mass index (BMI) >
  • •Hypertension.
  • •Uncontrolled diabetes mellitus.

研究组 & 干预措施

QLB group

Experimental

Patients will receive a quadratus lumborum block (QLB) using 20ml of bupivacaine 0.25%.

干预措施: Quadratus lumborum block (Other)

EXORA group

Experimental

Patients will receive an external oblique and rectus abdominis plane (EXORA) block using 20ml of bupivacaine 0.25%.

干预措施: External oblique and rectus abdominis plane block (Other)

结局指标

主要结局

Time to the 1st rescue analgesia

时间窗: 24 hours postoperatively

Time to the first request for the rescue analgesia (time from the end of surgery to first dose of morphine administrated).

次要结局

  • Total morphine consumption(24 hours postoperatively)
  • Intraoperative fentanyl consumption(Intraoperatively)
  • Degree of pain(24 hours postoperatively)
  • Incidence of adverse events(24 hours postoperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammed Said ElSharkawy

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.

Tanta University

研究点 (1)

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