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Comparison of voltage during pulsed radiofrequency of lumbar dorsal root ganglion in patient with lumbar radiculopathy

Not Applicable
Conditions
Diseases of the musculoskeletal system and connective tissue
Registration Number
KCT0007578
Lead Sponsor
Catholic Kwandong University International St.Mary's Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria

age =20 years old
- pain intensity =5 out of 11 on the numerical rating scale (NRS)
- chronic LRP lasting =12 weeks
- previous failure of conservative management such as physiotherapy, exercise therapy, or analgesic medications - lumbar spinal stenosis was confirmed on magnetic resonance imaging (MRI)
All eligible patients received conventional fluoroscopy-guided transforaminal epidural injection with local anesthetics and steroid before enrollment. Patients who demonstrated no pain reduction (NRS score =5) following epidural injection were finally enrolled.

Exclusion Criteria

- patient refusal
- age <20 years
- unbearable pain >9–points on NRS, pain <4–points on NRS
- acute pain of onset lasting <12 weeks
- signs of progressive motor weakness or neurologic deficits
- allergies to steroids or contrast dyes
- coagulopathy
- epidural steroid injection within the previous 4 weeks
- systemic infection, injection site infection
- malignancy

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
number of successful responders to treatment in each group at the 3-month follow-up period. Successful response was defined as: 1) =50% or 4-point reduction in the NRS pain intensity (or) 2) 10-point decrease in ODI, or mean score =6 points on the GPE scale
Secondary Outcome Measures
NameTimeMethod
RS pain intensity at 1, 2 4, 12 weeks and ODI scores at 4, 12 weeks post-procedure
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