The Effect of Additional Transforaminal Epidural Blocks in Percutaneous Epidural Neuroplasty

• Conditions: Lumbar Spinal Stenosis

• Registration Number: NCT03867630
• Lead Sponsor: Ajou University School of Medicine

Brief Summary

Percutaneous epidural neuroplasty (PEN) is an effective interventional treatment for radicular pain. But in some cases with wire catheter like Racz catheter, contrast runoffs were not shown to the foramen. This study will show that contrast runoff will affect the results of PEN and in cases which contrast runoff are not shown, additional transforaminal epidural blocks will affect the results of PEN by reviewing medical record, retrospectively.

Detailed Description

Medical records will be investigated in cases of PEN with wire type catheter from May 2016 to August 2018. About one hundred cases will be enrolled. Analysis will be performed. It will be compared 1) Success rate of Runoff group and Nonrunoff group in lumbar spine, 2) Success rate of Runoff group and Nonrunoff-NonTransforaminal group in lumbar spine. 3) Success rate of Runoff group with nonrunoff-transforaminal group and Nonrunoff-NonTransforaminal group in lumbar spine. 4) Success rate of Nonrunoff-Transforaminal group and Nonrunoff-NonTransforaminal group in lumbar spine.

Study Timeline

• Study First Submitted: 2019-03-05
• Study First Submitted QC: 2019-03-06
• Study First Posted: 2019-03-08
• Status Verified: 2019-05
• Study Start: 2019-05-10
• Last Update Submitted: 2019-05-10
• Last Update Posted: 2019-05-13
• Primary Completion: 2019-06-30
• Study Completion: 2019-06-30

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• 20 to 80 years old
• Patients with a herniated disc, spinal stenosis
• Patients with chronic low back pain and lower extremity pain who did not respond to lumbar epidural steroid injections
• Patients who are performed percutaneous epidural neuroplasty with wire type catheter.

Exclusion Criteria

• Incomplete medical record
• Contraindication to percutaneous epidural neuroplasty

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Success rate of three groups	1 month	Success rate of three groups(Runoff group, Nonrunoff-foraminal group, Nonrunoff-Nonforaminal group) will be compared each other. Success is defined as a 50% or greater reduction in pain score on the pre-procedural Visual Analogue Scale(VAS) score.