Efficiency Comparison Between Methylprednisolone and Phenol 8% Treatment Using a Trans Sacral Approach - on Lower Back Pain and Limbs
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ClinicalTrials.gov Identifier: NCT01468415
Recruitment Status : Unknown
Verified May 2011 by Assaf-Harofeh Medical Center. Recruitment status was: Recruiting
The American Society of Anesthesiologists Task Force on Management, Chronic Pain section, recommended Phenol neurolysis when other techniques have failed to provide adequate pain control. In this study we sought to Compare the pain relieve on a Lower Back and Limbs obtained from Methylprednisolone and Phenol 8% Treatment given by Trans Sacral Approach. The study includes patients who suffers from a chronic low back and/or limbs pain which were referred to be given epidural as a treatment. Control group receives 80 mg Methylprednisolone while the test group receives phenol 8%.
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Layout table for eligibility information
Ages Eligible for Study:
18 Years and older (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Inclusion Criteria: -at least 18 years of age;
chronic low back pain of at least 12 weeks duration;
patients which were diagnosed as a candidate for epidural since other techniques have failed to provide adequate pain control
Sciatica due to Lumbar Disc Herniation
Neurogenic Claudication due to Lumbar Spinal Stenosis
patients with unbalanced high blood pressure
patients who can not ley prone
patients who consumes anti-clotting medications
patients with bleeding problems
patients with Diabetes
patients who suffers from chronic non-specific lower back and limb pain