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临床试验/NCT02530775
NCT02530775撤回不适用

"Is Instrumentation Necessary for "Static" Degenerative Spondylolisthesis - A Prospective Randomized Clinical Study"

University of Pittsburgh0 个研究点开始时间: 2015年10月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
主要终点
Functional Outcome Scores: SF-12/SF-36 Quality of Life Questionnaires

研究概览

简要总结

The purpose of this study is to determine whether instrumented lumbar fusion provides superior clinical outcomes in comparison to non-instrumented fusion in patients with "static" degenerative spondylolisthesis.

详细描述

This study will determine whether instrumented lumbar fusion will provide superior clinical outcomes in comparison to non-instrumented fusion in patients with "STATIC" degenerative spondylolisthesis. At the time of scheduling surgery, patients who meet the inclusion/exclusion criteria will be asked to participate. Patients who agree, will be randomized to either non-instrumented or instrumented arthrodesis group. Intra-operative, peri-operative, and post-operative data will be collected and compared. The investigators predict to get very similar clinical outcomes between the two groups, with possibly less complications from the non-instrumented group and definitely a reduction in cost compared to the instrumented group.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Patients with stable L4-5 spondylolisthesis on lumbar flexion and extension radiographs. Stability will be determined by the treating physician.
  • Patients with concomitant spinal stenosis.
  • Laminectomy at any lumbar levels of stenosis.
  • Fusion only at L4-5 level.

排除标准

  • Prior lumbar spine surgery
  • Multi-level spondylolisthesis
  • Anterior interbody work/fusion

结局指标

主要结局

Functional Outcome Scores: SF-12/SF-36 Quality of Life Questionnaires

时间窗: Up to 2 years

Measured by patient outcome survey such as the SF-12 or SF-36 Questionnaire (all questions are scored on a scale from 0 to 100, with 100 representing the highest level of functioning possible)

Functional Outcome Scores: Oswestry Disability Index (ODI) Questionnaire

时间窗: Up to 2 years

Measured by patient outcome survey such as the Oswestry Disability Index (ODI) that assesses low back pain (scoring ranges from 0 to \>35)

次要结局

  • Rate of Infection(Expected average of 4 weeks)
  • Rate of Symptomatic Pseudoarthrosis(Up to 2 years)
  • Need for Revision Surgery(Up to 2 years)
  • Length of Hospital Stay(Expected average of 1 week)
  • Surgical Time(2-4 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Joon Yung Lee, MD

M.D.

University of Pittsburgh

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