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临床试验/NCT01365754
NCT01365754已完成不适用

Posterior Dynamic Stabilization Versus Fusion in the Treatment of Lumbar Degenerative Disease

Technical University of Munich1 个研究点 分布在 1 个国家目标入组 440 人开始时间: 2011年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
440
试验地点
1
主要终点
Difference in Oswestry disability index (ODI) between treatment groups at 2 years post intervention

研究概览

简要总结

The purpose of this study is to compare posterior dynamic stabilization with fusion in the treatment of lumbar degenerative disease.

详细描述

Two strategies for treatment of degenerative lumbar instability are in frequent clinical use: fusion versus dynamic stabilization. Up to now it is not clear whether fusion (Gold-standard) or the non-fusion technique is superior. Nevertheless some data are available that dynamic stabilization as a less invasive technique can achieve similar or better results concerning patient satisfaction and re-OP rate compared with fusion as the standard therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

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

入选标准

  • •Age >18 years
  • •Mono- or bisegmental symptomatic lumbar degenerative disease with or without stenosis
  • •Indication for fusion with (i) spondylolisthesis of at least 5mm or segmental vertebral motion of at least 3mm or 10º on flexion/extension radiographs, (ii) predominant low back pain in combination with Modic changes
  • •Failure of adequate conservative measures for more than 3 months
  • •Correctly signed informed consent form

排除标准

  • •Olisthesis more than grade I, spondylolisthesis vera, spondylolysis without olisthesis or spinal deformity (i.e. scoliosis of more than 20°, sagittal imbalance)
  • •Significant comorbidity impeding with surgical success (e.g. osteoporosis, rheumatoid arthritis, mental illness)
  • •Previous fusion or stabilization surgery

研究组 & 干预措施

B

Active Comparator

B - Dynamic (new)

干预措施: new (Procedure)

A

Active Comparator

A - Fusion

干预措施: standard (Procedure)

结局指标

主要结局

Difference in Oswestry disability index (ODI) between treatment groups at 2 years post intervention

时间窗: 2 years after intervention

次要结局

未报告次要终点

研究者

发起方
Technical University of Munich
申办方类型
Other
责任方
Sponsor

研究点 (1)

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