跳至主要内容
临床试验/NCT04996290
NCT04996290已完成不适用

Combined Pericapsular Nerve Group (PENG) and Lateral Femoral Cutaneous Nerve (LFCN) Block for Total Hip Arthroplasty: A Randomized Controlled Trial

University Hospital, Antwerp1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2020年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
1
主要终点
Initial pain score

研究概览

简要总结

A clinical trial investigating the effect of a combined locoregional anesthesia technique on the postoperative analgesia outcomes after a total hip arthroplasty. A PENG block will be used in combination with a LFCN block. The results will be compared to a control group that is solely treated with intravenous analgesia. This technique aims to provide improved pain scores after surgery without interference of revalidation.

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
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult patients who underwent a primary total hip replacement under general anesthesia

排除标准

  • insulin dependent diabetes mellitus
  • chronic pain
  • severe dementia or mental retardation
  • allergy to local anesthetics

研究组 & 干预措施

PENG + LFCN block

Active Comparator

The participants in this group received a combined regional technique just before surgery:

  • Pericapsular nerve group (PENG) block
  • Lateral femoral cutaneus nerve (LFCN) block

干预措施: PENG + LFCN block (Procedure)

PENG + LFCN block

Active Comparator

The participants in this group received a combined regional technique just before surgery:

  • Pericapsular nerve group (PENG) block
  • Lateral femoral cutaneus nerve (LFCN) block

干预措施: Ropivacaine injection (Drug)

结局指标

主要结局

Initial pain score

时间窗: 0 hours postoperative

numeric rating score (NRS) of 0 to 10

Pain score after 2h

时间窗: 2 hours postoperative

numeric rating score (NRS) of 0 to 10

Pain score after 24h

时间窗: 24 hours postoperative

numeric rating score (NRS) of 0 to 10

次要结局

  • Initial motor function(0 hours postoperative)
  • Motor function after 2h(2 hours postoperative)
  • Postoperative opioids(24 hours postoperative)
  • Intraoperative opioids(intraoperative)
  • Motor function after 24h(24 hours postoperative)

研究者

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

Lennert De Schrijver

Principal Investigator

University Hospital, Antwerp

研究点 (1)

Loading locations...

相似试验