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临床试验/NCT02196883
NCT02196883撤回不适用

A Prospective, Randomized, Single Blind Study Comparing Transforaminal Epidural Steroid Injections at the Level of MRI Pathology vs Clinical Symptoms

State University of New York - Upstate Medical University2 个研究点 分布在 1 个国家开始时间: 2014年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
试验地点
2
主要终点
Visual Analog Scale

研究概览

简要总结

Patients are being asked to participate in a research study because the patients are being treated for low back pain and the patients have decided to have an epidural steroid injection.

Low back pain has a tremendous impact on the individual and society. It not only affects the individuals quality of life, it also contributes to lost productivity and increased health care costs.

Epidural steroid injections (ESIs) are a common treatment option for many forms of low back pain. They have been used for low back problems since 1952 and are still being used as a non-surgical form of treatment for low back pain. The goal of the injections is reduction of pain, increased quality of life and improved function.

This study is being conducted to determine the outcomes of injections given at the "level of MRI Pathology" versus at the "level of clinical symptoms" to see if one is more effective than the other and to learn more about the characteristics of the two different injections.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
Single

入排标准

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

入选标准

  • Diagnosis of Single level spinal stenosis.
  • Single level radiculopathy with MRI findings at a different level than clinical pattern.
  • Chronic low back pain with radicular symptoms of > 4 weeks, but < 6 months.
  • Failure of conservative therapy to include physical and pharmacotherapy.
  • Patient is at least 21 years of age.
  • Patient is willing to be blinded to treatment until after the 3-month follow up visit.
  • Patient is willing and able to review and sign the study's informed consent form.

排除标准

  • Patient has a mental or physical condition that would invalidate evaluation results.
  • Patient has had prior lumbar surgery at any level.
  • Patient is pregnant.
  • Patient has systemic infection or infection at the proposed injection site.

结局指标

主要结局

Visual Analog Scale

时间窗: 2 weeks to 6months

次要结局

  • Oswestry Disability Index(2 weeks to 6months)
  • Short Form 36 Health Survey(2 weeks to 6months)

研究者

发起方
State University of New York - Upstate Medical University
申办方类型
Other
责任方
Sponsor

研究点 (2)

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