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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05176301
Other study ID # DaeguCUMC
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 8, 2021
Est. completion date July 12, 2021

Study information

Verified date March 2022
Source Daegu Catholic University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Cervical epidural block could cause spinal cord injury if the epidural needle is over-inserted and punctures the spinal cord. Investigators retrospectively evaluated the imaging data of 100 patients (50 men and 50 women) who underwent both cervical computed tomography (CT) and cervical magnetic resonance imaging (MRI) at our hospital. Investigators measured the diameters of the spinal canal and spinal cord from the 3rd cervical vertebra to the 1st thoracic vertebra (T1) at each level by using the patients' cervical CT and MR images. The spinal cord and spinal canal diameters were measured in the transverse plane of cervical MR and CT images, respectively.


Description:

The spinal canal diameter, i.e., the epidural transverse diameter, was measured as the distance between the innermost border of the left and right pedicles at each upper pedicular level from C3 to T1 on transverse CT images by using a picture archiving and communication system (PACS; INFINITT PACS G3, INFINITT Healthcare, Korea) The spinal cord diameter was measured between the left and right outermost distances of the cord at each upper pedicular level, which were almost the same locations used for measuring the spinal canal diameter, from C3 to T1 on transverse MR images by using the PACS.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date July 12, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria: - 100 patients (50 men and 50 women aged 20 to 70 years old) who visited our hospital and underwent both cervical CT and MRI simultaneously Exclusion Criteria: - patients who had a history of cervical spine surgery or cervical cord edema, whose CT or MR images did not include all the cervical vertebrae from C3 to T1, - patients who had at least one missing medical detail such as diagnosis, age, height, or weight.

Study Design


Related Conditions & MeSH terms


Intervention

Radiation:
computed tomography, Magnetic resonance image
Investigators measured the cervical cord and canal diameter by using CT and MRI that were previously taken.

Locations

Country Name City State
Korea, Republic of Daegu Catholic University Hospital Daegu

Sponsors (1)

Lead Sponsor Collaborator
Daegu Catholic University Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary the cord to canal diameter ratio the measurement of the cord to canal diameter ratio, i.e., the cord to epidural space diameter ratio of each cervical vertebral level from the 3rd cervical vertebra (C3) to the 1st thoracic vertebra (T1) in the coronal plane from December 1, 2020 through study completion, an average of 2 years were investigated retrospectively.
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