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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

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Yonsei University

Status

Completed

Conditions

Low Back Pain Due to Spinal Nerve Compression

Treatments

Procedure: skin compression

Study type

Interventional

Funder types

Other

Identifiers

NCT02281227
4-2014-0721

Details and patient eligibility

About

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

Enrollment

60 patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients with ≥ 25 kg/m2 BMI who were scheduled for the transforaminal epidural injection

Exclusion criteria

  • Local anesthetic allergy, coagulopathy

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

compression group
Active Comparator group
Description:
skin compression with an indicator for determination of needle entry point
Treatment:
Procedure: skin compression
non-compression group
Active Comparator group
Description:
non skin compression with an indicator for determination of needle entry point
Treatment:
Procedure: skin compression

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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