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临床试验/NCT06226675
NCT06226675Unknown不适用

The Effect of Adding Lateral Femoral Cutaneous Nerve Block to PENG Block on Postoperative Opioid Consumption in Hip Surgery

Zonguldak Bulent Ecevit University2 个研究点 分布在 2 个国家目标入组 60 人开始时间: 2023年1月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
2
主要终点
postoperative opioid consumption

研究概览

简要总结

The incidence of femoral neck fracture in Europe is 330/10000 per year. It is increasing every year due to the aging of the population. In patients 55 years and older, hip fracture-related mortality is estimated to be between 4% and 16% at one month and between 11% and 43% at one year after surgery. The reduced risk of postoperative complications associated with the use of regional anesthesia, shorter mobilization times, and reduced morphine consumption in hip fractures have been reported, and have been incorporated into postoperative pain control as part of multimodal strategies. PENG has been described for postoperative pain control for surgery on the hip joint or for the treatment of post-traumatic pain associated with proximal femur/femoral head fractures. Lateral femoral cutaneous nerve block is used in combination with other peripheral block methods to provide analgesia in the lateral thigh.

The investigators aimed to evaluate the effect of adding lateral femoral cutaneous nerve block to PENG block on pain scores and opioid consumption in femoral fracture procedures under spinal anesthesia.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-75 years old,
  • ASA I-II-III risk group
  • patients undergoing hip fracture surgery under spinal anesthesia
  • Patients whose informed consent was read and consent was obtained from them and their representatives.

排除标准

  • Those who do not want to participate in the study,
  • ASA IV-V patients
  • Those with coagulation disorders
  • Allergic to local anesthetics

结局指标

主要结局

postoperative opioid consumption

时间窗: up to 24 hour after surgery

total morphine requirement

次要结局

  • postoperative complications(up to 24 hour after surgery)
  • mobilization time(up to 24 hour after surgery)
  • pain scores(up to 24 hour after surgery)
  • first analgesic time(up to 24 hour after surgery)

研究者

发起方
Zonguldak Bulent Ecevit University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Keziban Bollucuoglu

Principal Investigator

Zonguldak Bulent Ecevit University

研究点 (2)

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