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临床试验/NCT06935006
NCT06935006尚未招募不适用

Sonographic Guided Erector Spinae Plane Block Versus Conventional Analgesia After Percutaneous Nephrolithotomy a Comparative Randomized Study

Sohag University0 个研究点目标入组 50 人开始时间: 2025年5月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
50
主要终点
Reduction of postoperative pain

研究概览

简要总结

50 adult patients scheduled for percutaneous nephrolithotomy in Sohag university hospitals will be devided in two groups one of them will receive Sonographic guided erector spinae plane block using 20 ml volume of bupivacaine 0.25 percent and the other will receive conventional analgesia of 0.1 mg/kg IV morphine

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, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA 1 to ASA 2 18 to 60 years

排除标准

  • patient refusal Significant neurological , psychiatric or neuromascular disease Drug abuse Pregnant or lactating women Suspected coagulopathy Morbid obesity Known allergy to some medications Septicaemia and local infection at block site

研究组 & 干预措施

Erector spinae plane block group

Active Comparator

干预措施: Sonographic guided Erector spinae plane block (Procedure)

Conventional analgesia group

Active Comparator

干预措施: Intravenous opioid (Drug)

结局指标

主要结局

Reduction of postoperative pain

时间窗: 1 year

VAS score for pain measurement

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

Ahmed Mahmoud Azmy

Assistant lecturer of Anaethesia and intensive care unit

Sohag University

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