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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02300714
Other study ID # 4-2014-0822
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date November 2014
Est. completion date July 14, 2015

Study information

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

Clinical Trial Summary

A comparison of anterioposterior versus oblique view approach method for fluoroscopically-guided epidural block in the midthoracic region. The investigators evaluate differences on total radiation time and technical feasibility between anterioposterior and oblique view approach method.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date July 14, 2015
Est. primary completion date July 14, 2015
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- Adult patients who were scheduled for the transforaminal epidural injection in midthoracic region (T5-T7)

Exclusion Criteria:

- Local anesthetic allergy, coagulopathy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
oblique view approach


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