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临床试验/NCT06976320
NCT06976320招募中不适用

Deep Rectus Sheath Block for Postoperative Analgesia in Patients Undergoing Laparoscopic Cholecystectomy

Istinye University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月9日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
60
试验地点
1
主要终点
Morphine consumption

研究概览

简要总结

Postoperative pain after laparoscopic cholecystectomy can be considerable. Regional techniques such as erector spinae plane (ESP) block or transversus abdominis plane (TAP) block may be suitable for patients at increased risk of postoperative pain. The deep rectus sheath block is a novel block which is a modified version of the conventional rectus sheath block. It was reported in a few case reports that, it may be used for postoperative analgesia in patients undergoing laparoscopic cholecystectomy. The aim of this study is to investigate the postoperative analgesic efficacy of deep rectus sheath block in patients undergoing laparoscopic cholecystectomy.

详细描述

Patients scheduled for elective laparoscopic gastrectomy will be separated into 2 groups: Control Group and Deep Rectus Sheath Block Group. Patients in Control Group will be received patient controlled analgesia with morphine for postoperative analgesia. Patients in Deep Rectus Sheath Block Group will be performed Deep Rectus Sheath Block at the end of the surgery, along with patient controlled analgesia with morphine for postoperative analgesia. Morphine consumption for first postoperative 24 hours, numerical rating scale scores, amount of rescue analgesic drug, incidence of postoperative nausea and vomiting will be recorded.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 80 years
  • Patients with American Society of Anesthesiology (ASA) physical status I-II
  • Patients scheduled for a laparoscopic cholecystectomy

排除标准

  • Allergy to local anesthetics
  • Coagulopathy
  • Skin infection at the deep rectus sheath block area
  • Advanced hepatic or renal failure
  • Chronic pain syndromes
  • Alcohol or drug abuse
  • Severe pulmonary and/or cardiovascular disease
  • Psychiatric disorders

结局指标

主要结局

Morphine consumption

时间窗: Postoperative 24 hours

The amount of morphine required by the patient and given by the device will be recorded for the first 24 hours.

次要结局

  • Postoperative numerical rating scale scores(Postoperative 24 hours)
  • Rescue analgesic drug requirement(Postoperative 24 hours)
  • Incidence of postoperative nausea and vomiting(Postoperative 24 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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