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NCT02281227

Determination of a Proper Needle Entry Point; Effects of Skin Compression With an Indicator on Radiation Exposure Time of Fluoroscopically Guided Transforaminal Epidural Block in Obese Patients

Completed NA Last updated 22 February 2019
What this trial tests

NA trial testing skin compression in Low Back Pain Due to Spinal Nerve Compression in 60 participants. Completed in 10 October 2015.

Timeline
20 October 2014
Primary endpoint
10 October 2015
10 October 2015

Quick facts

Lead sponsorYonsei University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment60
Start date20 October 2014
Primary completion10 October 2015
Estimated completion10 October 2015
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Yonsei University

Who can join

Adults 20 to 80, any sex, with Low Back Pain Due to Spinal Nerve Compression. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To evaluate the effects of skin compression with an indicator at the needle entry point on radiation exposure time of fluoroscopically guided transforaminal epidural block in obese patients

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Yonsei University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02281227.

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