Clinical Trials Directory

Trials / Unknown

UnknownNCT02597244

Effectiveness of Percutaneous Foraminotomy

Effectiveness of Percutaneous Foraminotomy in Patients With Lumbar Foraminal Stenosis: A Prospective, Pilot Study

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Seoul National University Hospital · Academic / Other
Sex
All
Age
45 Years – 85 Years
Healthy volunteers
Not accepted

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.

Detailed description

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

Conditions

Interventions

TypeNameDescription
DEVICEPercutaneous Extraforaminotomypercutaneous dissecting of the lumbar extraforaminal and foraminal region with BS extraforamonotomy kit(BioSpine Co.,Ltd, Seoul, South Korea) under fluoroscopy

Timeline

Start date
2014-06-01
Primary completion
2016-01-01
Completion
2016-01-01
First posted
2015-11-05
Last updated
2015-11-05

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02597244. Inclusion in this directory is not an endorsement.