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临床试验/NCT04542720
NCT04542720招募中不适用

Decompression Versus Decompression and Fusion for Lumbar Adjacent Segment Disease

Massachusetts General Hospital1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
96
试验地点
1
主要终点
Physical Function, short form 10a (SF10a)

研究概览

简要总结

Adjacent segment disease (ASD) in the lumbar spine is a well-known sequela of lumbar fusion surgery. The annual incidence of adjacent level re-operation is approximately 3% with a ten-year prevalence of 20-30%. Frequently, the surgical treatment involves decompression of the adjacent level coupled with extension of the instrumentation and fusion. Advocates of this paradigm cite the altered kinematics and biomechanics of levels adjacent to a lumbar fusion mass. Furthermore, decompressed levels adjacent to a fused segments are associated with higher rates of ASD in retrospective studies. Yet, a retrospective review of higher quality data concluded decompression adjacent to single-level fusion provides similar outcomes compared to fusions extending across the decompressed segments.

Given the conflicting data currently available, higher quality data are needed to guide surgical decision-making in ASD. The purpose of this trial is to prospectively compare decompression and decompression with fusion in patients with lumbar ASD.

研究设计

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

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

  • Adult patients at least one year removed from a previous instrumented posterior lumbar fusion
  • Patients with any prior posterior fusion involving L2 to the sacrum, whether single-level or multilevel
  • Patients with symptoms related to central and lateral recess at the supradjacent level that have persisted despite at least six weeks of non-operative therapy modalities

排除标准

  • Patients with previous uninstrumented lumbar fusions
  • Patients with traumatic, neoplastic, or infectious etiologies at the adjacent segment
  • Patients with prior iliac or sacroiliac fixation and those with nonunion as the primary indication for surgery
  • Patients with pre-existing instability at the supradjacent level. The definition of instability will be determined based on standing lateral, flexion and extension plain radiographs. Patients with >3mm of change between these views will be excluded.
  • Retrolisthesis will not be a criterion for exclusion

结局指标

主要结局

Physical Function, short form 10a (SF10a)

时间窗: 3 months, 6 months, 1 year, and 2 years post-operation

Scored by Patient-Reported Outcomes Measurement Information System (PROMIS): 0-62 (higher score = better outcome)

Global Health, Physical

时间窗: 3 months, 6 months, 1 year, and 2 years post-operation

Scored by Patient-Reported Outcomes Measurement Information System (PROMIS): 16-68 (higher score = better outcome)

次要结局

  • Global Health, Mental(3 months, 6 months, 1 year, and 2 years post-operation)
  • Anxiety, short form 4a (SF4a)(3 months, 6 months, 1 year, and 2 years post-operation)
  • Depression, short form 4a (SF4a)(3 months, 6 months, 1 year, and 2 years post-operation)
  • Pain interference, short form 4a (SF4a)(3 months, 6 months, 1 year, and 2 years post-operation)
  • Hospital length of stay(3 months, 6 months, 1 year, and 2 years post-operation)
  • Post-operative narcotic utilization(3 months, 6 months, 1 year, and 2 years post-operation)
  • Pain intensity, short form 3a (SF3a)(3 months, 6 months, 1 year, and 2 years post-operation)
  • Post-operative complication(3 months, 6 months, 1 year, and 2 years post-operation)

研究者

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

Daniel G.Tobert, M.D.

Principle Investigator

Massachusetts General Hospital

研究点 (1)

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