Lumbar Spinal Stenosis Clinical Trial
Official title:
A Randomized Trial in Patients With Lumbar Spinal Stenosis, Comparing the Order of Treatment With Epidural Corticosteroid Injections and Physical Therapy
Verified date | February 2017 |
Source | Emory University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Patients with back pain with spinal stenosis of the lower back will be asked to volunteer for this research study. These patients don't need immediate surgery for this problem. Treatment of this kind of back pain with spinal stenosis usually includes physical therapy exercises and steroid injections. Both treatments are usually helpful in patients with back pain with spinal stenosis. However, physicians and other healthcare providers don't know which treatment is better to give first. The purpose of this research is to answer that question. Patients enrolled in this study will receive both treatments: physical therapy (PT) and a steroid injection ("shot"). However, patients may get the shot first followed by PT, or they may have PT first, followed by the shot. Their time in this study will last up to 6 months, and there will be five outcome measurements (via visits or telephone). All study visits will take place at the Atlanta VA Medical Center (Atlanta VA). Investigators hope to enroll about 120 subjects from the Atlanta VA. Enrolled patients will be randomized using a randomization computer program.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2017 |
Est. primary completion date | January 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: chronic low back pain (at least 3 months in duration), a Visual
Analogue Scale (VAS) greater than 30 (on a 100 point scale), between the ages of 18 to 80
years, either without radiating leg pain (below the knees) or with low back and/or buttock
pain greater than leg pain (in which case the VAS for leg pain must be 20 or less),
ability to read English and complete the assessment instruments, and diagnosis of lumbar
spinal stenosis by a board certified radiologist or a board certified physiatrist either
by magnetic resonance imaging (MRI) or computed-tomography (CT) that has previously been
done as part of a normal course of patients medical treatment. All underlying etiology or
diagnoses that are the source for lumbar spinal stenosis will be recorded (e.g.
spondylolisthesis, herniated or degenerative discs, spondylosis). Exclusion Criteria: - history of lumbar surgery, acute disc herniation as reported on a radiologic imaging report, acute or severe chronic illness that are unstable, cognitive impairment which prevents the patient from providing accurate data or giving informed consent, neurological conditions (e.g. stroke, Parkinson's, brain injury), lower extremity amputees, fibromyalgia or chronic generalized pain, unstable opioid use or any signs or evidence of alcohol dependence or illicit drug use (as determined by screening questionnaire), clinical suspicion of facet joint-originating back pain or a positive response to prior facet joint block, lumbar epidural steroid injections within the last 6 months, uncontrolled psychiatric disorders, serious concomitant medical illness (e.g. acute heart failure, acute renal failure) or severe pain that may impair patient's ability to participate in physical therapy exercises or pain that is deemed so severe such that withholding of an ESI until after completion of the PT exercises is seen as causing unreasonable suffering to the patient, and conditions that would prevent the patient from undergoing fluoroscopy (e.g. pregnancy). |
Country | Name | City | State |
---|---|---|---|
United States | Atlanta Veterans Affairs Medical Center | Decatur | Georgia |
Lead Sponsor | Collaborator |
---|---|
Emory University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Oswestry disability Index | measurements will be done at baseline, week 4 (1-2 weeks after intervention), 6 months, and at 1 year | 1 year | |
Secondary | visual analog scale | measurements will be done at baseline, week 4 (1-2 weeks after intervention), 6 months, and at 1 year | 1 year |
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