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CompletedNCT05176301Updated Apr 1, 2022

Cervical Cord to Canal Diameter Ratio

An observational study in Cervical Pain, sponsored by Daegu Catholic University Medical Center. Completed at 1 site in Korea, Republic of. Open to participants aged 20 Years to 70 Years. Per ClinicalTrials.gov, last updated 2022-04-01.

Sponsored by Daegu Catholic University Medical Center · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
100
Ages
20 Years to 70 Years
Sex
All
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Study 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.

Read the detailed 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.

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Conditions studied

  • Cervical Pain

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Keywords

  • Coronal
  • Cervical canal diameter
  • Cervical cord diameter
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In context

Neck Pain

1,360 studies on the registry are indexed under Neck Pain; 299 are open to participants now.

This study's enrollment of 100 is above the median of 90 across 226 observational studies indexed under Neck Pain.

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Lead sponsor

Daegu Catholic University Medical Center is the lead sponsor of 28 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
20 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

patients who visited Daegu catholic university hospital

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

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

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.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
100 participants (actual)
Patient registry
No

Interventions

  • Radiationcomputed tomography, Magnetic resonance image

    Investigators measured the cervical cord and canal diameter by using CT and MRI that were previously taken.

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What researchers measure

Primary outcomes

  1. 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

    Time frame: from December 1, 2020 through study completion, an average of 2 years were investigated retrospectively.

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Study locations

1 site
  • Daegu Catholic University Hospital
    Daegu, Korea, Republic of
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 1, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05176301
Lead sponsor
Daegu Catholic University Medical Center
Responsible party
Jin Yong Jung (Professor, Daegu Catholic University Medical Center) — Principal investigator
First posted
Jan 4, 2022
Start date
Jun 8, 2021
Primary completion
Jun 30, 2021
Completion
Jul 12, 2021
Last update
Apr 1, 2022

Study contacts

Jin Y Jung, M.D.
study chair · Daegu Catholic University Medical Center

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2022. You cannot join it, but the record below documents what was studied.

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