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临床试验/NCT02897336
NCT02897336撤回不适用

Ultrasound-guided Caudal or Interlaminar Injection? A Comparative Study of Epidural Corticosteroid Injections in the Treatment of Lumbar Disk Herniation-related Sciatica

University Hospital, Caen2 个研究点 分布在 1 个国家开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
lower limbs pain

研究概览

简要总结

An open-label randomized trial to compare the efficacy of ultrasound-guided caudal and interlaminar corticosteroid injections for the treatment of lumbar disk herniation-related sciatica.

详细描述

An open-label randomized trial conducted in one centre to compare the efficacy of ultrasound-guided caudal and interlaminar corticosteroid injections for the treatment of lumbar disk herniation-related sciatica. 30 male and female patients will be included in each group. The primary outcome measure will be a 30% decrease in lower limbs pain as assessed by a visual analog scale.

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

  • radicular pain (sciatica or cruralgia) for more than 2 weeks
  • failure of analgesics and NSAIDs
  • without neurological deficiency (motor weakness lower or equal to 3/5)
  • a lumbar disk herniation on MRI or CT dating less than 3 months

排除标准

  • history of lumbar surgery
  • history of epidural injection during the last 3 months
  • radicular pain not due to disk herniation
  • a contraindication to epidural injection (infection, diabetes)
  • history of allergic reaction to corticosteroid
  • patient under legal guardianship

结局指标

主要结局

lower limbs pain

时间窗: day 15

a 30% decrease in lower limbs pain using a visual analog scale

次要结局

  • Oswestry questionnaire(day 15 - month 1 - month 3 - month 6)
  • medical outcome(day 15 - month 1 - month 3 - month 6)
  • resumption of work(day 15 - month 1 - month 3 - month 6)
  • A decrease of radicular pain with a pain numerical scale lower or equal to 3/10(day 15 - month 1 - month 3 - month 6)
  • neurological deficiency assessed by neurological examination(day 15 - month 1 - month 3 - month 6)
  • drugs(day 15 - month 1 - month 3 - month 6)
  • number of patients with treatment-related adverse events as assessed by CTCAE v4.0(day 15 - month 1 - month 3 - month 6)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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