Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT07456137

Prospective Evaluation of Upright Versus Supine CT Myelography of the Lumbar Spine

The purpose of this prospective study is to compare the diagnostic utility of standing (upright, weight-bearing) CT myelography with standard supine CT myelography for the evaluation of lumbar central canal and neural foraminal stenoses. This study aims to determine whether upright positioning provides additional diagnostic information in patients unable to undergo MRI, with the goal of improving assessment and management of degenerative lumbar spine disease.

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

The University of Kansas Medical Center

Kansas City, Kansas, 66160, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • Outpatient status
  • Scheduled for routine supine CT myelography

Exclusion criteria

  • Inpatient status
  • Presence of metallic lumbar spinal hardware
  • History of osseous metastatic disease involving the lumbar spine
  • Acute traumatic injury involving the lumbar spine
  • Pregnancy
  • Participant body habitus exceeding the scanner's safe operational limits (e.g., gantry/bore size clearance, table weight capacity) as defined by the device manufacturer.
  • Inability to tolerate CT scanning (e.g., severe pain, unable to stand independently for an extended period)

Treatment and study plan

Upright CT

Radiation

Upright CT Myelography

Other names: Upright CT Myelography

Primary outcomes

  1. Does upright CT imaging change management plans for patients with lumbar spinal stenosis

    Time frame: 1 week

    To determine whether upright CT imaging changes the management plan (yes or no) for patients with lumbar spinal stenosis.

Secondary outcomes

  1. Spine measurements

    Time frame: 1 day

    Objective measurements at different angles (mm) will be taken of the spine.

  2. Severity grading of central canal stenosis

    Time frame: 1 day

    Severity grading (mild, moderate, severe) of central canal stenosis in the spine.

  3. Severity grading of neural foraminal stenosis

    Time frame: 1 day

    Severity grading (mild, moderate, severe) of neural foraminal stenosis in the spine.

  4. Presence or absence of nerve root compression

    Time frame: 1 day

    Presence or absence of nerve root compression in the spine.

  5. Presence or absence of disc bulges

    Time frame: 1 day

    Presence or absence of disc bulges in the spine.

  6. Presence or absence of herniations

    Time frame: 1 day

    Presence or absence of herniations in the spine.

Sponsors and collaborators

Lead sponsor

University of Kansas Medical Center

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 6, 2026
Registry last updated
Jul 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.