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临床试验/NCT01335646
NCT01335646已完成不适用

Surgery Versus Standardized Non-operative Care for the Treatment of Lumbar Disc Herniations: A Canadian Trial

The London Spine Centre2 个研究点 分布在 1 个国家目标入组 128 人开始时间: 2010年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
128
试验地点
2
主要终点
Visual Analogue Scale for leg pain intensity

研究概览

简要总结

The objective of this study is to determine if surgery is superior to non-operative care for sciatica caused by a lumbar disc herniation. This study will include patients that have had severe sciatica for greater than 4 months which reflects the wait time of the Canadian health care system. This study is an opportunity to make an important contribution to medical science as there is no "top tier" evidence for or against this highly prevalent surgery. Although there have been several recent randomized trials in the field, all have been marred by a large number of patient crossing over from non-operative to operative treatment. Due to the wait for spine surgery, the Canadian system has a built-in delay that prevents such a cross over of patients. This study capitalizes on this unique opportunity to perform a high caliber surgical trial. Patients consenting to be in the study will be randomly assigned to expedited surgery within three weeks or standardized non-operative care while they wait on the surgeons list for consultation and then surgery (minimum wait of 9 months). The study will assess pain, function, quality of life, satisfaction, and work status to determine if one treatment is superior.

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18 - 60 years old
  • Unilateral, single L5 or S1 radiculopathy (leg pain following dermatomal distribution of L5 or S1)
  • Leg dominant pain over central back pain
  • Positive straight leg raise <70 degrees
  • MRI with corresponding L4-5 or L5-S1 posterolateral disc herniation*
  • Radicular symptom duration greater than 4 months and less than 12 months. May be recurrent if first episode occurred within 12 months and duration of presenting episode is greater than 4 months.
  • Agree to possible discectomy

排除标准

  • Radiculopathy secondary to foraminal stenosis
  • Radiculopathy secondary to intra-foraminal or far lateral disc herniation
  • Radiculopathy secondary to lumbar central or lateral recess stenosis not caused by a posterolateral disc herniation
  • Previous lumbar surgery at involved level
  • Lumbar spondylolisthesis or lateral listhesis at level of disc herniation
  • Lumbar Scoliosis greater than 10 degrees

结局指标

主要结局

Visual Analogue Scale for leg pain intensity

时间窗: 6 months

(Scale 0-10: 0 = no pain, 10 worst pain)

次要结局

  • Visual Analogue Scale for central back pain intensity(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • Visual Analogue Scale for leg pain frequency(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • Visual Analogue Scale for central back pain frequency(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • Visual Analogue Scale for leg pain intensity(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • Satisfaction with treatment (% of patients satisfied with treatment)(6 weeks, 3 months, 6 months, 1 year)
  • Oswestry Disability Index(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • SF36 - Generic Health Outcome Measure(enrollment, 6 weeks, 3 months, 6 months, 1 year)
  • Return to Work Status (% of patients employed)(enrollment, 6 weeks, 3 months, 6 months, 1 year)

研究者

发起方
The London Spine Centre
申办方类型
Other
责任方
Sponsor

研究点 (2)

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