跳至主要内容
临床试验/NCT05817916
NCT05817916已完成不适用

Comparison of Erector Spina Plane Block and Lumbar Plexus Block for Postoperative Analgesia in Femoral Fracture Surgery

Sakarya University2 个研究点 分布在 2 个国家目标入组 64 人开始时间: 2023年4月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
64
试验地点
2
主要终点
Postoperative opioid consumption

研究概览

简要总结

The aim is to clinical trials compare the lumbar plexus block method with the erector spinae plan block method in terms of analgesic efficacy and possible complications. İn patients for femur fracture surgery. The main questions it aims to answer are: 1. is erector spinae plane block as effective as lumbar plexus block for postoperative analgesia in femur fractures? 2. Is erector spinae plane block effective for reducing opioid consumption compared to lumbar plexus block?

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
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Proximal femoral surgery
  • All patients who can respond to pain assessment questions

排除标准

  • Regional block contraindications,
  • Severe cardiac and respiratory disease,
  • Severe coagulopathy,
  • Body mass index greater than 35

结局指标

主要结局

Postoperative opioid consumption

时间窗: postoperative 24 hours

Opioid consumption will be measured in micrograms.

次要结局

未报告次要终点

研究者

发起方
Sakarya University
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验