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临床试验/KCT0006198
KCT0006198招募中未知

Evaluation of the efficacy and safety of conventional and interlaminar full-endoscopic decompressive laminectomy to treat lumbar spinal stenosis (ENDO-F Trial): A prospective, randomized, Assessor blind, multicenter trial

The Catholic University of Korea, Seoul St. Mary's Hospital0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
120

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 80(Year)(—)
性别
All

入选标准

  • A. 20 to 80 years old
  • B. Those who have a grade of B or higher for lumbar central canal stenosis and who choose to perform 1-2 segment posterior decompression
  • C. Those who can follow up for more than 1 year
  • D. Research subject who signed the consent form after fully understanding the contents of the clinical trial by the principal (if signature is possible)

排除标准

  • A. Meyer Gr II or higher spondylolisthesis
  • B. Those who have previously performed the same segmental surgery
  • C. Lumbar degenerative scoliosis (Cobb angle> 20 degrees)
  • D. If the cause of the stenosis is not degenerative or due to an intervertebral disc herniation
  • E. If there is another spinal disease in the affected area of lumbar stenosis (ankylosing spondylitis, tumor, compression fracture, etc.)
  • F. Psychiatric diseases (dementia, mental retardation, severe drug addiction, etc.)
  • G. Those who refused to participate in the study
  • H. Other patients who are in charge of clinical trials as unsuitable for clinical trials

研究者

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