跳至主要内容
临床试验/TCTR20191229003
TCTR20191229003尚未招募不适用

Does direct decompression necessary for Lateral Lumbar Interbody Fusion (LLIF)?: A randomize control trial

Department of Orthopaedics Faculty of Medicine Chulalongkorn University0 个研究点目标入组 24 人开始时间: 2019年12月29日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
50 Years 至 80 Years(—)
性别
All

入选标准

  • Age between 50 and 80 years
  • - Patients who suffered from low back pain and/or leg pain with neurogenic intermittent claudication and progressive neurological deficit and confirmed to have single level lumbar stenosis, spondylolisthesis, or herniated nucleus pulposus (HNP) any level between L2-L5 by radiographical examinations
  • - Persistent complaints for at least 3 months, regardless of conservative treatments

排除标准

  • - Motor power less than grade III
  • - Cauda equina syndrome
  • - Spinal tumor
  • - Spinal infection
  • - Spinal fractures
  • - Previous surgery at L2 to L5 level
  • - Can not perform OLIF: No corridor, Previous retroperitoneal surgery
  • - More than one level that needs fusion

研究者

发起方
Department of Orthopaedics Faculty of Medicine Chulalongkorn University

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