跳至主要内容
临床试验/NCT01057641
NCT01057641终止4 期

A Clinical Study on the Treatment of Degenerative Lumbar Spine Stenosis With a Percutaneous Interspinous Implant in Comparison With the Best Non-operative Treatment of Lumbar Spine Stenosis

University of Cologne4 个研究点 分布在 1 个国家目标入组 22 人开始时间: 2011年3月最近更新:
适应症

试验速览

阶段
4 期
状态
终止
入组人数
22
试验地点
4
主要终点
Changes in subscores for bodily pain and physical function on SF-36

研究概览

简要总结

Neurogenic intermittent claudication is a specific symptom complex occurring in patients with lumbar spinal stenosis. Characteristic of this disease is the occurrence of increasing leg, buttock or groin pain with or without lower back pain when walking a certain distance or reclining. Bending forward or sitting leads to a rapid pain relief. Lumbar spinal stenosis is defined as a reduction of the diameter of the spinal canal. The mechanism leading to stenosis is a remodeling and overgrowth of the spinal canal with osteophyte formation. Any loss of tissue or decrease of the disc height results in a relative laxity of the ligament structures and accelerates the degeneration of the spinal joints. As a therapy option, conservative therapy with oral analgesics and physical therapy is considered. This treatment can be intensified by adding epidural pain treatment. Is the conservative treatment not successful surgical intervention is necessary. In patients over 65 years of age operative decompression of the lumbar spinal stenosis constitutes the most common surgical operation of the spine. A relatively new therapy alternative is the interspinous process decompression (IPD). Studies have shown that the IPDs prevent narrowing of the spinal canal and neural foramens. The study is intended as a randomised, monocentre study to investigate the safety and the benefit of a minimally invasive percutaneous IPD-device in comparison with the best non-surgical operative treatment of lumbar spinal stenosis.

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
50 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female over 50 years of age
  • One, two, or three segment degenerative lumbar spinal stenosis (DLSS)
  • Symptoms of radiographically confirmed DLSS like leg, buttock, or groin pain with or without back pain and absence of a peripheral motoric deficit
  • Pain relief in inclination or sitting
  • Ability to walk over a distance of 50 m
  • Unsuccessful conservative therapy for 3 months under outpatient conditions
  • Informed consent

排除标准

  • Fixed motoric deficit
  • Cauda equina syndrome
  • Previous surgery of the lumbar spine
  • Severe osteoporosis of the vertebrae and/or of the hip
  • Spondylolisthesis more severe than Meyerding I (on scale of I-IV)
  • Metastasis of the vertebrae
  • Mentally disabled persons

结局指标

主要结局

Changes in subscores for bodily pain and physical function on SF-36

时间窗: baseline, 6 months

次要结局

  • Physical function by applying ZCQ(baseline, 6 months)
  • General health status (Quality of life) by applying SF-36(baseline, 6 months)
  • Post-treatment patient satisfaction by applying ZCQ(baseline, 6 months)
  • Symptoms severity by applying the Zurich Claudication Questionaire (ZCQ)(baseline, 6 months)
  • Measurement of walking distance(baseline, 6 months)

研究者

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

Dr. Gregor Stein

Dr. med

University of Cologne

研究点 (4)

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