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临床试验/NCT01885481
NCT01885481已完成不适用

Evaluation of Efficacy and Safety of Epidural Steroid Injection Using Dexamethasone or Betamethasone in Patients With Spinal Pain: a Prospective, Randomized, Double-blind Study

Seoul National University Bundang Hospital1 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2013年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
600
试验地点
1
主要终点
the proportion of patients with pain improvement

研究概览

简要总结

Particle steroid drug such as triamcinolone has been used widely for epidural steroid injection (ESI) treatment in Korea. However, Korea FDA recently prohibit ESI using triamcinolone, following the regulation of US FDA. Therefore, dexamethasone and betamethasone become only candidate drugs for ESI in Korea and the investigators are curious about the effectiveness and safety of both drugs due to limitation of information about comparison of two drugs in previous literature. So, this study aims to compare the effectiveness and safety of both drugs and our hypothesis is that there is no difference of the effectiveness between dexamethasone and betamethasone at 2 weeks after ESI.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • patients with spinal pain (i.e.neck pain, back pain, or radiculopathy..)
  • patients with informed consent
  • visual analog scale (VAS) is five or more in 10-point scale at screening
  • sustained spinal pain, regardless of sufficient conservative treatment (i.e. oral medicine, physical therapy..)

排除标准

  • age of patient less than 19 years
  • relative contraindication of epidural steroid injection, as follows:
  • pregnant or breast-feeding state
  • uncontrolled coagulopathy
  • suspected of active infection state
  • uncontrolled diabetes mellitus
  • previous history of adverse event related to epidural steroid injection

研究组 & 干预措施

ESI-1

Active Comparator

epidural steroid injection using dexamethasone

干预措施: Dexamethasone (Drug)

ESI-2

Experimental

epidural steroid injection using betamethasone

干预措施: Betamethasone (Drug)

结局指标

主要结局

the proportion of patients with pain improvement

时间窗: baseline and 2 weeks

the proportion of patients with significant pain improvement at 2 week after epidural steroid injection, with the patients' subjective satisfaction scale of "much improved" or "no pain"

次要结局

  • incidence of adverse events(during 12 weeks after epidural steroid injection)
  • disability improvement(baseline and 2 weeks)
  • pain relief(baseline and 2 weeks)

研究者

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

Joon Woo Lee

Associate professor, Department of Radiology

Seoul National University Bundang Hospital

研究点 (1)

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