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临床试验/NCT01267825
NCT01267825终止4 期

A Randomized Trial of CT-guided Perineural Injection With a Corticosteroid Plus a Long Acting Local Anesthetic Versus Standard Medical Management in Patients With Acute Lumbar Radiculopathy and a Corresponding Disc Herniation

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2010年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
终止
入组人数
1
试验地点
1
主要终点
Change in Functional Impairment as Measured by the Roland Morris Disability Questionnaire

研究概览

简要总结

Herniated disc sometimes cause back pain radiating down to a leg. This pain can be so severe that it is functionally disabling. The purpose of this randomized clinical trial is to determine if corticosteroid medication, delivered directly to the area near the herniated disc, can improve the pain and functional disability associated with a herniated disc.

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
21 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Adults <60y
  • < 1m of symptoms
  • Symptoms consistent with herniated disc
  • MRI demonstrates corresponding disc
  • Back pain resulting in functional disability

排除标准

  • Chronic pain
  • Daily pain medication
  • Frequent back pain
  • On the job injury

研究组 & 干预措施

Standard medical care

Active Comparator

干预措施: Standard medical care (Drug)

CT-guided intervention

Experimental

CT guided perineural injection of corticosteroid+ bupivicaine Also get typical medical care

干预措施: CT-guided corticosteroid+ bupivicaine (Drug)

结局指标

主要结局

Change in Functional Impairment as Measured by the Roland Morris Disability Questionnaire

时间窗: Baseline and one week after emergency department discharge

The Roland Morris Disability Questionnaire (RMDQ) is a 24 item instrument that evaluates the impact of low back pain on one's daily life. It is most sensitive for patients with mild to moderate disability due to acute, sub-acute or chronic low back pain. Each question can be answered as either a "yes" or "no". The score ranges from 0 to 24 where a higher score reflects greater impairment and, therefore, worsening in the quality of life. The change in RMDQ is obtained by subtracting the RMDQ score at one week after discharge from the baseline score. The calculated mean and associated confidence interval values have been verified by staff statisticians.

次要结局

  • Adverse Events(1 week after discharge from emergency department)
  • Functional Disability Assessed Using Roland-Morris Scale(1 month)

研究者

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

Benjamin W. Friedman, MD

Prof. Emergency Medicine

Montefiore Medical Center

研究点 (1)

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