Clinical Trials Directory

Trials / Unknown

UnknownNCT01468415

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

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Assaf-Harofeh Medical Center · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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%.

Conditions

Interventions

TypeNameDescription
DRUGphenol1 cc of 8% phenol dissolved in water or 20cc of 8o mg Methylprednisolone diluted in 0.25% marcaine.

Timeline

Start date
2011-06-01
Primary completion
2013-06-01
First posted
2011-11-09
Last updated
2011-11-09

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01468415. Inclusion in this directory is not an endorsement.