跳至主要内容
临床试验/NCT02962206
NCT02962206已完成不适用

The Effect of Point-of-care Ultrasound Guidance for Distal Radius Fracture Reduction

Marcus Van Aarsen4 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2017年1月10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
22
试验地点
4
主要终点
Residual dorsal angulation

研究概览

简要总结

Distal radius (Colle's) fractures in adult patients are commonly reduced in the emergency department before casting. Standard of care currently requires that x-rays be performed before and after fracture reduction, and inadequate reductions may be subject to repeat attempts and are at a higher risk to require surgery. This study will assess the use of point-of-care ultrasound (POCUS) in addition to standard care as a tool to decrease the angulation at the fracture site after a reduction is performed. If this angulation is decreased, it would suggest that POCUS for distal radius fracture reduction could decrease the number of failed reduction attempts and therefore the number of repeated reduction attempts.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • radiographically confirmed distal radius fracture

排除标准

  • patients who do not consent
  • patients with multiple acute injuries, open fractures, or other local fractures evident (a simple ulnar styloid fracture will not be considered an exclusion criterion)
  • patients with neurovascular compromise
  • patients with bilateral distal radius fractures
  • patients with minimally displaced distal radius fractures that do not require closed reduction before casting

结局指标

主要结局

Residual dorsal angulation

时间窗: Collected at the same-day post-reduction xray. Data will be aggregated over 1 year

次要结局

  • Physician satisfaction: post-reduction questionnaire(Questionnaire to be administered immediately after reduction. Data to be aggregated during the 1 year study period)
  • Need for orthopaedic surgery within 6 weeks of injury(To be assessed 6 weeks post-injury. Data will be aggregated over the 1 year study period)

研究者

发起方
Marcus Van Aarsen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Marcus Van Aarsen

Resident Physician

Western University, Canada

研究点 (4)

Loading locations...

相似试验