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临床试验/NCT00786981
NCT00786981已完成不适用

Epidural Steroid Injection Versus Epidural Steroid Injection and Manual Physical Therapy and Exercise in the Management of Lumbar Spinal Stenosis; a Randomized Clinical Trial

Franklin Pierce University7 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2009年4月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
54
试验地点
7
主要终点
The primary outcome of interest will be change in disability as measured by the Modified Oswestry Disability Index (OSW).

研究概览

简要总结

Lumbar spinal stenosis (LSS) is a prevalent and disabling condition in the rapidly growing aging population. People with LSS often have a substantial physical and psychosocial burden as well as significant healthcare costs affecting both the individual and society. It has been reported that patients with LSS over the age of 65 are more likely to undergo spinal surgery than any other condition with an estimated total annual inpatient expense of one billion. Individuals undergoing surgical treatment for LSS tend to be older, therefore operative morbidity and mortality are a particular concern. Functional benefit derived from conservative treatment may increase the health and quality of life for individuals suffering from LSS and avoid or delay the need for surgery in some subjects. As the population continues to age, identifying effective non-surgical treatment options for older patients with LSS is an important research priority. Ultimately, the information gained from this study will help fill a significant void in medical literature regarding non-surgical options for this patient population.

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
50 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Lumbar spinal stenosis unidentified by MRI or CT scan and interpreted by a radiologist independent of the study. The criteria of Boden et al will be used to define LSS on MRI: non-discogenic loss of signal in the epidural fat with compression of neural tissues.
  • Chief complaint of pain in the low back, buttock, and/or lower extremity. The patient must have LE symptoms consistent with neurogenic claudiation.
  • Patient-reported inability to walk greater than ¼ mile due to lower extremity pain and/or cramping.
  • Rates sitting as a better position with respect to symptom severity compared to standing or walking.
  • Consent of the patient to undergo education, epidural steroid injection(s), and attend specified physical therapy sessions.
  • Individuals with no language barrier, that are cooperative, have transportation to the Spine Center, and who sign an informed consent form.
  • Age greater than or equal to 50 years.

排除标准

  • Patients with organic brain syndrome or dementia.
  • Severe vascular, pulmonary or coronary artery disease which limits ambulation.
  • Recent myocardial infarction (within last 6 months).
  • Spondylolisthesis requiring surgical fusion (i.e., greater than 5mm of slippage).
  • Previous spinal surgery that included fusion of two or more vertebrae.
  • Severe osteoporosis as defined by multiple compression fractures or a fracture at the same level as the stenosis.
  • Metastatic cancer.
  • Excessive alcohol consumption or evidence of non-prescribed or illegal drug use.

研究组 & 干预措施

Epidural steroid injection and physical therapy

Other

干预措施: Epidural steroid injection plus physical therapy (Other)

Epidural steroid injection

Other

干预措施: Epidural steroid injection (Other)

结局指标

主要结局

The primary outcome of interest will be change in disability as measured by the Modified Oswestry Disability Index (OSW).

时间窗: 10 weeks, 6 months, 12 months

次要结局

  • Change in patient satisfaction(10 weeks, 6 months, 12 months)
  • Change in Functional Limitations(10 weeks, 6 months, 12 months)
  • Change in patient-reported pain(10 weeks, 6 months, 12 months)
  • Change in psychosocial evaluation(10 weeks, 6 months, 12 months)

研究者

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

Joshua Cleland, DPT, OCS

Professor

Franklin Pierce University

研究点 (7)

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