Effectiveness of Percutaneous Foraminotomy

Status Recruiting

Clinical Trial Summary

Percutaneous Extraforaminotomy using BS extraforamonotomy kit(BioSpine Co.,Ltd, Seoul, South Korea), was performed in patients who did not show improvement lasting more than 1 month after diagnostic conventional fluoroscopically guided transforaminal epidural block with local anesthetic and steroid.

Numeric rating scale(NRS) pain score, Oswestry disability index (ODI), Roland-Morris Disability Questionnaire (RDQ), claudication distance(CD) was checked before and after the procedure.

Clinical Trial Description

Percutaneous Extraforaminotomy with Transforaminal Adhesiolysis may be an effective minimal invasive technique in patients not responsive to conventional epidural steroid injection. ;

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02597244
Study type	Interventional
Source	Seoul National University Hospital
Contact	Sangchul Lee, MD, PhD
Phone	+82-2-2072-2248
Email	pain8275@gmail.com
Status	Recruiting
Phase	N/A
Start date	June 2014
Completion date	January 2016

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