跳至主要内容
临床试验/NCT07537036
NCT07537036招募中不适用

Analgesic Efficacy of Quadro-Iliac Plane Block Versus Erector Spinae Plane in Total Hip Arthroplasty: A Randomized Non-Inferiority Trial

Tanta University1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2026年4月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
76
试验地点
1
主要终点
Time to the first rescue analgesia

研究概览

简要总结

This study aims to compare the Quadro-Iliac Plane Block versus Erector Spinae Plane Block after total hip arthroplasty.

详细描述

Total hip arthroplasty (THA) is frequently utilized in elderly patients to address hip pain and restore joint function. Effective postoperative pain management is critical; however, the use of opioids is associated with a range of adverse effects, including nausea, vomiting, pruritus, constipation, respiratory depression, and the risk of dependence.

Quadro-iliac plane block (QIPB) has been introduced, combining elements of both posterior and anterior QLB approaches.

Erector Spinae Plane Block (ESPB) was initially described as an analgesic approach for managing thoracic neuropathic pain. This innovative fascial block technique enables sensory blockade across multiple abdominal and thoracic wall segments.

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 Anesthesiology (ASA) physical status I-III.
  • Undergoing total hip arthroplasty (THA) under spinal anesthesia.

排除标准

  • History of allergies to local anesthetics.
  • Opioid dependency.
  • Body mass index (BMI) > 35 kg/m
  • Cognitive impairment.
  • Bleeding or coagulation disorders.
  • Psychiatric and neurological disorder.
  • Local infection at the site of injection.
  • Severe heart, lung, liver, and renal dysfunction.
  • Emergency surgery.

研究组 & 干预措施

QIPB group

Experimental

Patients will receive ipsilateral Quadro-iliac plane block (QIPB) using 20ml of bupivacaine 0.25%.

干预措施: Quadro-iliac plane block (Other)

ESPB group

Experimental

Patients will receive ipsilateral erector spinae plane block (ESPB) using 20ml of bupivacaine 0.25%.

干预措施: Erector spinae plane block (Other)

结局指标

主要结局

Time to the first rescue analgesia

时间窗: 24 hours postoperatively

Time to the first request for the rescue analgesia will be recorded from the end of surgery to first dose of morphine administrated.

次要结局

  • Total morphine consumption(24 hours postoperatively)
  • Degree of pain(24 hours postoperatively)
  • Quality of recovery(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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