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临床试验/KCT0002280
KCT0002280进行中(未招募)未知

Effects of combined percutaneous epidural adhesiolysis and balloon decompression in patients with refractory chronic low back and leg pain

Asan Medical Center0 个研究点目标入组 457 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
入组人数
457

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational Study

入排标准

年龄范围
20(Year) 至 100(Year)(—)
性别
All

入选标准

  • 1.Patients who visited pain clinic complained of lumbar radicular pain with or without lower back pain and the patients who agree to participating in this study.
  • 2.Adults patients over 20 years old.
  • 3.The patients with chronic (at least 3 months) lumbar radicular pain with or without lower back pain
  • 4.The history, clinical symptoms, lumbar magnetic resonance imaging (MRI) findings, and epidurogram revealed that filling defect was consistent with lesion.
  • 5.Refractory to conservative treatment (above 3 months)
  • 6.Patients who did not have pain relief for more than 1 month after epidural steroid injection or transforaminal epidural steroid injection as 1st line treatment.
  • 7.Patients who have voluntarily agreed in writing to participate in this study.

排除标准

  • 1.The patient does not agree to participate in the study
  • 2.Pregnant or lactating patients
  • 3.Side effects on topical anesthetics or steroids
  • 4.unbearable pain, NRS 10
  • 5.Red flag sign such as infection, cancer, neurologic deficit, and newly developed severe medical problem.
  • 6.Yellow flag (depression, anxiety, somatization, hypochondriasis, sue, claims)
  • 7.Uncontrolled medical condition

研究者

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