Effect of lumbar transforaminal epidural block with high volume injectate without steroids in patients with lumbar spinal stenosis: a randomized, controlled trial
Not Applicable
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0009196
- Lead Sponsor
- Ewha Womans University Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 52
Inclusion Criteria
Patients diagnosed with spinal stenosis and undergoing lumbar transforaminal epidural nerve block
Exclusion Criteria
Patients with a history of lumbar interforaminal epidural nerve block within 4 weeks before or after the procedure, patients taking oral steroids, cognitive dysfunction, taking anticoagulants, or patients and guardians who do not consent to the study.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score (VAS) the Roland-Morris disability questionnaire , Questionnaire for medical outcome short form health survery
- Secondary Outcome Measures
Name Time Method pain score(VAS) during procedure and spread pattern of contrast