The aim of this study is to evaluate the effectiveness of the use of systemic corticosteroids
administered orally in narrow lumbar canal syndrome.
Drug: predinose oral
Drug: placebo group
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Locations near you
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Full eligibility criteria for NCT01456377
Ages eligible for Study
50 Years to 75 Years
Genders eligible for Study
Accepts Healthy Volunteers
Low back pain and at least two of the following complaints in lower limbs: pain, weakness, burning or numbness that worsens with walking and improves with the cessation of walking.
decompensated diabetes mellitus.
Systemic hypertension and decompensated heart
systemic disease affecting the lower limbs
Use of steroids in the past 3 months.
Patients with previous surgery of the thoracic or lumbar spine.
cognitive disorder that interferes with the ability to understand or interpret the questionnaires
Spondylolisthesis except degenerative
degenerative scoliosis with Cobb angle of 10 °
All locations for NCT01456377
Santa Marcelina Hospital
São Paulo, Sao paulo, Brazil, 08270-070
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Santa Mareclina Hospital
Sao Paulo, Brazil, 08270-070
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View full eligibility
Tris trial is registered with FDA with number: NCT01456377. The sponsor of the trial is Federal University of São Paulo and it is looking for 60 volunteers for the current phase.
Official trial title: A Prospective Controlled Study Randomized Double Blind Study, Evaluate the Effectiveness of Oral Corticosteroids in the Treatment of Stenosis of Lumbar Canal In Symptomatic Patients
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