Effects of combined percutaneous epidural adhesiolysis and balloon decompressio

Not Applicable

Active, not recruiting

• Conditions: Diseases of the nervous system

• Registration Number: KCT0002280
• Lead Sponsor: Asan Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 March 2019

Recruitment & Eligibility

• Status: Active, not recruiting
• Sex: All
• Target Recruitment: 457

Inclusion Criteria

1.Patients who visited pain clinic complained of lumbar radicular pain with or without lower back pain and the patients who agree to participating in this study.
2.Adults patients over 20 years old.
3.The patients with chronic (at least 3 months) lumbar radicular pain with or without lower back pain
4.The history, clinical symptoms, lumbar magnetic resonance imaging (MRI) findings, and epidurogram revealed that filling defect was consistent with lesion.
5.Refractory to conservative treatment (above 3 months)
6.Patients who did not have pain relief for more than 1 month after epidural steroid injection or transforaminal epidural steroid injection as 1st line treatment.
7.Patients who have voluntarily agreed in writing to participate in this study.

Exclusion Criteria

1.The patient does not agree to participate in the study
2.Pregnant or lactating patients
3.Side effects on topical anesthetics or steroids
4.unbearable pain, NRS 10
5.Red flag sign such as infection, cancer, neurologic deficit, and newly developed severe medical problem.
6.Yellow flag (depression, anxiety, somatization, hypochondriasis, sue, claims)
7.Uncontrolled medical condition

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
umerical Rating scale;Os-Westry functional scale;7-ponit scale global perceived effect of satisfaction

Secondary Outcome Measures

Name	Time	Method
medication quantification scale III (MQS)