Determination of a Proper Needle Entry Point; Effects of Skin Compression With an Indicator on Radiation Exposure Time of Fluoroscopically Guided... | NCT02281227 | Trialant
CompletedInterventionalNot ApplicableUpdated Feb 22, 2019
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
ClinicalTrials.gov ID
NCT02281227
Lead Sponsor
Yonsei UniversityOTHER
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
60Actual
Last Update Posted
Feb 22, 2019Actual
Start Date
Oct 20, 2014Actual
Primary Completion Date
Oct 10, 2015Actual
Completion Date
Oct 10, 2015Actual
Brief Summary
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
Low Back Pain Due to Spinal Nerve Compression
skin compression
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients with ≥ 25 kg/m2 BMI who were scheduled for the transforaminal epidural injection
Exclusion Criteria:
Local anesthetic allergy, coagulopathy
Primary Purpose
Other
Allocation
Randomized
Interventional Model
Parallel Assignment
Masking
Single
No central contacts
There are no central contacts for this study.
Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine