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临床试验/NCT06837532
NCT06837532已完成不适用

Ultrasound Guided Versus Surgical Rectus Sheath Block Versus Local Anesthesia Infiltration for Postoperative Analgesia in Patients Undergoing Total Abdominal Hysterectomy: A Randomized Trial

Ain Shams University1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2025年2月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
90
试验地点
1
主要终点
Total morphine consumption

研究概览

简要总结

The aim of this work is to compare the efficacy and safety of the effectiveness and safety of ultrasound-guided surgical rectus sheath block and local anesthetic infiltration for postoperative analgesia in patients undergoing total abdominal hysterectomy.

详细描述

Total abdominal hysterectomy (TAH) is a commonly performed major surgical procedure that results in substantial postoperative pain and discomfort.

Local anesthetic infiltration (LAI) at the end of surgery is one of the most common technique employed in laparotomies for postoperative analgesia.

Rectus sheath block (RSB) has been used as a part of multimodal analgesia, especially when neuraxial techniques are unsuitable.The RSB was used to achieve peri-operative relaxation of the anterior 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
None

入排标准

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

入选标准

  • •Age from 18 to 65 years old.
  • •American Society of Anesthesiologists (ASA) physical status I - II.
  • •Patients scheduled for elective total abdominal hysterectomy under general anesthesia.

排除标准

  • •Hepatic, renal or cardiac disease.
  • •Any known allergy to local anesthetic.
  • •Physical or mental conditions which may vaguely measure postoperative pain following surgery.
  • •History of chronic use of analgesic as nonsteroidal anti-inflammatory drugs (NSAIDs) or central nervous system (CNS) depressants as antiepileptic, and bleeding disorders.

研究组 & 干预措施

Ultrasound-guided rectus sheath block group

Experimental

Patients will receive ultrasound-guided rectus sheath block (20 ml bupivacaine 0.25%) bilaterally at the end of surgery.

干预措施: Ultrasound-guided rectus sheath block (Drug)

Local anesthesia infiltration group

Experimental

Patients will receive local anesthesia infiltration at the end of surgery.

干预措施: Local anesthesia infiltration (Drug)

Surgical rectus sheath block group

Experimental

Patients will receive a surgical rectus sheath block (20 ml bupivacaine 0.25%) bilaterally at the time of closure.

干预措施: Surgical rectus sheath block (Drug)

结局指标

主要结局

Total morphine consumption

时间窗: 24 hours postoperatively

Rescue analgesia of morphine will be given as 3 mg bolus if the Visual Analogue Scale (VAS)\> 3 to be repeated after 30 min if pain persists until the VAS \< 4.

次要结局

  • Heart rate(Till the end of surgery (Up to 4 hours))
  • Mean arterial pressure(Till the end of surgery (Up to 4 hours))
  • Time to the first request for the rescue analgesia(24 hours postoperatively)
  • Degree of pain(24 hours postoperatively)
  • Degree of patient satisfaction(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

Sarah Ahmed

Lecturer of Anesthesia, Intensive care, and pain management, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

Ain Shams University

研究点 (1)

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