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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02281227
Other study ID # 4-2014-0721
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 20, 2014
Est. completion date October 10, 2015

Study information

Verified date February 2019
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date October 10, 2015
Est. primary completion date October 10, 2015
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

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

Exclusion Criteria:

- Local anesthetic allergy, coagulopathy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
skin compression
skin compression with an indicator for determination of needle entry point

Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total radiation exposure time Total radiation exposure time during whole epidural procedure. immediately =1 sec after the confirmation of successful epidural injection
Secondary The number of the needle readjustments The number of the needle readjustments for successful epidural injection immediately =1 sec after the confirmation of successful epidural injection