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临床试验/NCT07272577
NCT07272577招募中不适用

Efficacy of Erector Spinae Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Abdominal Surgeries

Assiut University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年12月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
Time to the 1st rescue analgesia

研究概览

简要总结

This study aims to evaluate the efficacy of the erector spinae plane block (ESPB) on postoperative analgesia in patients undergoing laparoscopic abdominal surgeries.

详细描述

Laparoscopic surgery is associated with less pain, fewer wound infections, reduced hospital stay, reduced morbidity and mortality, and early return to work and improved overall quality of life.

The role of ESPB as a better analgesic modality in reducing 24-hour opioid consumption has recently been established for post-operative analgesia in breast surgeries, video-assisted thoracoscopic surgery, and cardiothoracic surgeries.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥ 18 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I-II.
  • Body mass index (BMI) between 20-30 kg/m
  • Patients undergoing laparoscopic abdominal surgeries under general anesthesia.

排除标准

  • Bleeding or coagulation disorders.
  • Having local sepsis, pre-existing.
  • Peripheral neuropathies.
  • Chronic pain conditions.
  • Having any contraindication to regional anesthesia administration.
  • Opioid dependency.
  • Hypertension.
  • Uncontrolled diabetes mellitus.

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

  • Degree of pain(24 hours postoperatively)
  • Total morphine consumption(24 hours postoperatively)
  • Mean arterial pressure(Till the end of surgery (Up to 2 hours))
  • Heart rate(Till the end of surgery (Up to 2 hours))
  • 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

Bahaa Gamal Saad Mohamed

Anesthesia and Intensive Care, Faculty of Medicine, Assiut University, Assiut, Egypt.

Assiut University

研究点 (2)

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