跳至主要内容
临床试验/NCT05466110
NCT05466110招募中不适用

sPinal coRd stimulatiOn coMpared With Lumbar InStrumEntation for Low Back Pain After Previous Lumbar Decompression (PROMISE): a Prospective Randomized Controlled Study

University Hospital Augsburg2 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2023年3月20日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
84
试验地点
2
主要终点
Oswestry disability index / ODI

研究概览

简要总结

Low back pain affects people of all ages and has become the leading cause of living with disability worldwide. Patients, suffering from persistent pain after spinal surgery in the absence of any clear spinal pathology are defined of having a "failed back surgery syndrome (FBSS)" and treatment of FBSS remains a great controversy in the spinal community. Apart from conservative treatment, spinal fusion remains as therapeutic option. Furthermore, minimal invasive Neuromodulation techniques might be a promising alternative. Aim of this randomized interventional multi center study is to compare treatment success in FBSS patients with either spinal cord stimulation (SCS) or fusion surgery, 12 months after intervention according to the Oswestry Disability Index (ODI) and other scales and scores. Radiological and health economic outcome also will be analysed for thorough comparison of techniques. Additionally, the safety of the interventions needs to be compared.

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
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

  • Age ≥18 years
  • Symptomatic degenerative disc disease with LBP as a predominant symptom for at least 6 months following pervious surgery for disc herniation
  • ODI score at least 21
  • Correctly signed informed consent form

排除标准

  • Spinal stenosis resulting in spinal claudication or neurological deficits
  • Spinal Instability (> 3 mm Motion on dynamic Lumbar X-rays)
  • Major psychiatric disorder

结局指标

主要结局

Oswestry disability index / ODI

时间窗: 12 months after intervention

A patient reported outcome measure to rate pain and disability

次要结局

  • Pain medication(12 months after intervention)
  • hospital length of stay(through study completion, an average of 2 years)
  • Adverse events(12 months after intervention)
  • SF36(12 months after intervention)
  • EuroQOL 5D(12 months after intervention)
  • Crossover rates(12 months after intervention)

研究者

发起方
University Hospital Augsburg
申办方类型
Other
责任方
Sponsor

研究点 (2)

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