跳至主要内容
临床试验/KCT0000500
KCT0000500已完成未知

The effect of transforaminal ventral epidural hypertonic adhesiolysis in patients with epidural adhesion

Asan Medical Center0 个研究点目标入组 68 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
68

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20(Year) 至 85(Year)(—)
性别
All

入选标准

  • 1)Aged 20 years or older
  • 2)Chronic lumbosacral radiculopathy secondary to spinal stenosis
  • 3)Symptoms lasting for more than 12 weeks
  • 4)Dominant leg pain with less severe back pain
  • 5)Unilateral leg pain with the symptom restricted to one-level of dermatome
  • 6)Failure of conservative management
  • 7)Prior epidural injections not within 12 weeks before recruitment are permitted
  • 8)Correlation between the clinically determined level of radiculopathy and the confirmed findings on the MRI

排除标准

  • 1)NRS pain score >9 or <4
  • 2)Signs of progressive motor weakness or neurologic deficits
  • 3)Acute back or leg pain within 12 weeks
  • 4)Allergic response to steroid or contrast dye
  • 5)Bilateral radiculopathy, spondylolisthesis, multi-level spinal stenosis
  • 6)History of prior spine surgery
  • 7)Injection of steroids or hyaluronic acids within previous 12 weeks
  • 8)Radiographic confirmation of severe central canal stenosis
  • 9)Systemic infections, injection site infection
  • 10)Unstable medical or psychiatric condition
  • 11)Coagulopathy

研究者

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