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临床试验/NCT04749095
NCT04749095Unknown不适用

Can Bilateral Erector Spinae Plane Block Minimize Perioprative Opioid Consumption and Provide Satisfactory Analgesia for Lumbar Spine Fusion Surgery? A Randomized Controlled Study

Benha University0 个研究点目标入组 45 人开始时间: 2021年5月最近更新:
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适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
45
主要终点
Analgesia
研究概览研究设计入排标准研究组 & 干预措施结局指标研究者记录与标识符相似试验

研究概览

简要总结

The purpose of this study was to investigate the effect of a bilateral ultrasound guided erector spinae plane block on the pain scores and opoid utiliziation in fusion surgery of the lumbar spine.

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
Single (Participant)

入排标准

年龄范围
20 Years 至 65 Years（Adult, Older Adult）
性别
All
接受健康志愿者
是

入选标准

  • •American Society of Anesthesiologists class I-III adult patients
  • •BMI less than or equal 35 kg/m2

排除标准

  • •Patient refusal
  • •unable to give consent
  • •age < 18 or > 65
  • •BMI more than 35 kg/m2
  • •known allergy to the study medication
  • •coagulopathies or on anticoagulant medications
  • •hepatic insufficiency
  • •renal insufficiency
  • •chronic opioid use

研究组 & 干预措施

Erector block

Active Comparator

干预措施: Erector spinae plane block (Drug)

sham block

Active Comparator

干预措施: sham subcutaneous infiltration (Drug)

结局指标

主要结局

Analgesia

时间窗: Up to 24 hours after surgery

Numerical rating scale of pain every 6 hours

次要结局

未报告次要终点

研究者

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

Baher Said Elshahat Mohamed Abdelhady

Principal Investigator

Benha University

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