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Pain Relief as a postoperative functional outcome predictor in degenerative lumbar spinal stenosis

Not Applicable
Completed
Conditions
Diseases of the nervous system
Registration Number
KCT0006192
Lead Sponsor
Daegu Catholic University Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
60
Inclusion Criteria

1. Symptoms of single-level lateral recess or foraminal stenosis, with neurological and MRI findings matching the symptoms
2. Lesions determined as described above that are consistent with the lesions in which pain is provoked by the pricking of the spinal needle during SNRB
3. Symptomatic relief after early SNRB and recurrence of symptoms to a degree requiring surgical treatments
4. Completion of at least 2 years of follow-up after surgical treatment
5. Severe radiculopathy (LANSS > 7)
6. No signs of motor weakness

Exclusion Criteria

Lumbar herniated intervertebral discs, spondylolisthesis, tumor, infection, or trauma
Secondary gain such as work compensation or traffic accident compensation
Inability to communicate properly
History of surgery or SNRB

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
VAS of lower leg radiating pain
Secondary Outcome Measures
NameTimeMethod
Functional outcome( ODI, RMDQ ), Quality of life (SF-36 PCS, SF-36 MCS)
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