跳至主要内容
临床试验/NCT07047469
NCT07047469招募中不适用

Ultrasound-assisted Spinal Anesthesia in Midline Versus Paramedian Approach in Adult Orthopedic Surgery

Sohag University1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2025年6月13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
110
试验地点
1
主要终点
The severity of back pain in patients that will receive spinal anesthesia by median versus paramedian approach

研究概览

简要总结

This study aims to compare between the two methods (midline and paramedian approach of spinal anesthesia guided by ultrasound) by the number of needle passes required to successful dural puncture.

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
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients will perform orthopedic surgery
  • •Physical state I or II according to ASA classification
  • •Age between (18 - 50 )
  • •Body mass index less than 30

排除标准

  • •Patient refusal .
  • •Local infection at the puncture site .
  • •Allergy to any of the drugs to be administrated .
  • •Old age patients
  • •Obese patients
  • •Previous spinal surgery .
  • •Spinal stenosis .
  • •Multiple sclerosis .
  • •Coagulopathy.
  • •Hypovolemia .
  • •Systemic infection .
  • •Aortic stenosis .
  • •Spina bifida and back deformity .

研究组 & 干预措施

Group (1): spinal anesthesia with median approach

Active Comparator

patients undergoing orthopedic surgery will receive spinal anesthesia with median approach under ultrasound guided techniques

干预措施: Group (1): spinal anesthesia with median approach (Procedure)

Group (2): spinal anesthesia with paramedian approach

Active Comparator

patients undergoing orthopedic surgery will receive spinal anesthesia with paramedian approach under ultrasound guided techniques

干预措施: Group (2): spinal anesthesia with paramedian approach (Procedure)

结局指标

主要结局

The severity of back pain in patients that will receive spinal anesthesia by median versus paramedian approach

时间窗: 24 hours, 72 hours, and 1 week after spinal anesthesia.

pain measurement by numerical rating scale (NRS)

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

Areej Mohamed Abdelkader

Resident, Department of Anesthesia, Intensive Care and Pain management, Faculty of Medicine, Sohag University

Sohag University

研究点 (1)

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