跳至主要内容
临床试验/NCT03867630
NCT03867630Unknown不适用

The Effect of Additional Transforaminal Epidural Blocks in Percutaneous Epidural Neuroplasty With Wire Type Catheter in Lumbar Foraminal Stenosis Patients

Ajou University School of Medicine0 个研究点目标入组 100 人开始时间: 2019年5月10日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
100
主要终点
Success rate of three groups

研究概览

简要总结

Percutaneous epidural neuroplasty (PEN) is an effective interventional treatment for radicular pain. But in some cases with wire catheter like Racz catheter, contrast runoffs were not shown to the foramen. This study will show that contrast runoff will affect the results of PEN and in cases which contrast runoff are not shown, additional transforaminal epidural blocks will affect the results of PEN by reviewing medical record, retrospectively.

详细描述

Medical records will be investigated in cases of PEN with wire type catheter from May 2016 to August 2018. About one hundred cases will be enrolled. Analysis will be performed. It will be compared 1) Success rate of Runoff group and Nonrunoff group in lumbar spine, 2) Success rate of Runoff group and Nonrunoff-NonTransforaminal group in lumbar spine. 3) Success rate of Runoff group with nonrunoff-transforaminal group and Nonrunoff-NonTransforaminal group in lumbar spine. 4) Success rate of Nonrunoff-Transforaminal group and Nonrunoff-NonTransforaminal group in lumbar spine.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 20 to 80 years old
  • Patients with a herniated disc, spinal stenosis
  • Patients with chronic low back pain and lower extremity pain who did not respond to lumbar epidural steroid injections
  • Patients who are performed percutaneous epidural neuroplasty with wire type catheter.

排除标准

  • Incomplete medical record
  • Contraindication to percutaneous epidural neuroplasty

结局指标

主要结局

Success rate of three groups

时间窗: 1 month

Success rate of three groups(Runoff group, Nonrunoff-foraminal group, Nonrunoff-Nonforaminal group) will be compared each other. Success is defined as a 50% or greater reduction in pain score on the pre-procedural Visual Analogue Scale(VAS) score.

次要结局

未报告次要终点

研究者

发起方
Ajou University School of Medicine
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jong Bum Choi

Assistant Professor

Ajou University School of Medicine

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