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临床试验/NCT05600244
NCT05600244招募中不适用

Comparison of Pericapsular Nerve Group Block, Quadratus Lumborum Block and Lumbar Erector Spinae Plane Block for Acute Pain Management in Total Hip Surgery: A Randomized Clinical Trial

Kafrelsheikh University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年12月15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
60
试验地点
2
主要终点
Total amount of rescue analgesia

研究概览

简要总结

The aim of this study is to compare between Pericapsular Nerve Group Block, Erector Spinae Plane Block and Quadratus Lumborum Block for managing acute postoperative pain in patients undergoing total hip surgeries under spinal anesthesia.

详细描述

Total hip surgeries are one of the most common major orthopedic procedures to improve patient's functional status and quality of life. However, despite these advantages, the immediate postoperative period can be associated with severe pain that delays mobilization and increases hospital stay and the risk of thromboembolic events.

Various methods are used for postoperative pain management. Intravenous opioid agents are among them, but they may cause undesirable side effects, such as respiratory depression, sedation, constipation, allergic reaction, nausea, and vomiting. Thus, alternative techniques are preferred.

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
All
接受健康志愿者

入选标准

  • Age 18-65 years
  • Both genders
  • Body mass index < 40 kg/m^2
  • American Society of Anesthesiologists (ASA) physical status I-III
  • Posted for total hip surgeries under spinal anesthesia

排除标准

  • The presence of contraindications or allergy to local anesthetic agents
  • Chronic use of opioids or corticosteroids
  • Infection at the puncture site
  • Coagulopathy
  • Psychiatric disorders (dementia or cognitive impairment.

结局指标

主要结局

Total amount of rescue analgesia

时间窗: 24 hours postoperatively

Total amount of rescue analgesia in the form of morphine will be recorded

次要结局

  • First analgesic request(24 hours Postoperatively)
  • Adverse events(48 hours Postoperatively)
  • Pain level(48 hours Postoperatively)

研究者

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

Mohamed Fouad Algyar

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine

Kafrelsheikh University

研究点 (2)

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