Overview

Efficiency Comparison Between Methylprednisolone and Phenol 8% Treatment Using a Trans Sacral Approach - on Lower Back Pain and Limbs

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
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%.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Assaf-Harofeh Medical Center
Treatments:
Methylprednisolone
Methylprednisolone acetate
Methylprednisolone Hemisuccinate
Phenol
Prednisolone
Prednisolone acetate
Prednisolone hemisuccinate
Prednisolone phosphate
Criteria
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

Exclusion Criteria:

- 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