跳至主要内容
临床试验/NCT04062474
NCT04062474已完成不适用

Treatment of Pain in Patients With Lumbar Spinal Stenosis By Epidural Intervention of Spinal Nerves With Local Anesthetic, Steroids and Tumor Necrosis Factor-Alpha Inhibitor Respectively:a Prospective Randomized Study

Nanjing First Hospital, Nanjing Medical University0 个研究点目标入组 90 人开始时间: 2016年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
90
主要终点
Oswestry Disability Index

研究概览

简要总结

This study is to assess the clinical efficacy of epidural injections with Tumor Necrosis Factor-Alpha(TNF-α) Inhibitor in patients with chronic radicular pain caused by lumbar spinal stenosis.

详细描述

This study is to assess the clinical efficacy of epidural injections with Tumor Necrosis Factor-Alpha(TNF-α) Inhibitor in patients with chronic radicular pain caused by lumbar spinal stenosis.Ninety patients were diagnosed with lumbar spinal stenosis and were randomly assigned to 3 groups, for each group 30 cases. Patients in Group A received epidural injection of spinal nerve with 2.0 ml of lidocaine and 10 mg of Tumor Necrosis Factor-Alpha Inhibitor (etanercept) onto the affected spinal nerve, Group B patients received epidural injection with lidocaine 2ml mixed with 2ml of steroid(Diprospan), and group C patients received epidural injections with 4.0 ml of lidocaine only. All the 3 groups were evaluated by VAS and ODI, and received 6 months' follow-up.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of spinal stenosis with radicular pain at least 5 scores of VAS(ranging from 0 to 10).
  • Failed to improve symptom significantly through conservative treatment, including physiotherapy, chiropractic therapy, exercise, medication and bed rest.

排除标准

  • lumbar surgery history,
  • spinal stenosis without radicular pain,
  • uncontrollable or unstable use of opioids,
  • uncontrolled mental illness,
  • pregnant or lactating women,
  • patients with a history of adverse reactions or possible adverse reactions to local anesthetics, etanercept or Steroids.

结局指标

主要结局

Oswestry Disability Index

时间窗: 6 months

Oswestry Disability Index is for movement function, Questionnaire examines

visual analog scale

时间窗: 6 months

visual analog scale(0-10 scores) is for pain, 0 represent no pain, 10 score represent the severe pain.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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