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Recruiting NCT06436716

Artificial Intelligence Model for Traumatic Cervical Spinal Cord Injury Based on Radiomics and Genomics

Observational Spinal Cord Injuries

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: MRI.
Who it may be relevant to
Registry conditions: Spinal Cord Injuries. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Second Affiliated Hospital of Nantong University, Nantong First People's Hospital, Nantong University

Overview

Collect standardized, structured, and comprehensive disease-specific information, produce high-quality and accurate clinical data, provide a sample basis for the analysis and mining of spinal cord injury clinical big data, and establish a spinal cord injury-specific disease data platform to serve clinical work. Promote multi-center cooperation in spinal cord injury research: Establish a unified, standardized, queryable, and sharable efficient spinal cord clinical research data platform to promote multi-center cooperation in spinal cord injury clinical research and enhance the international competitiveness of this research field. Help the region to prepare for the establishment of a spinal cord injury-specific disease data platform for various hospitals in the region, forming a spinal cord injury-specific disease network center to achieve data sharing.

Interventions

  • Radiation MRI
    Every patient needs an MRI to assess spinal cord injury. This is one of the clinically necessary examinations.

Primary outcome measures

  • MRI image [Time frame: From 2016 to 2027]
  • ASIA scores [Time frame: From 2016 to 2027]
Secondary outcome measures (5)
  • Age [Time frame: From 2016 to 2027]
  • Gender [Time frame: From 2016 to 2027]
  • Weight [Time frame: From 2016 to 2027]
  • Height [Time frame: From 2016 to 2027]
  • BMI [Time frame: From 2016 to 2027]

Eligibility criteria

Inclusion criteria

  • MRI Diagnosis of TCSCI
  • Clinic Diagnosis of TCSCI
  • The injury site must be in cervical spinal cord
  • MRI images of T2WI must be collected within 48 hours after injury
  • Complete and available imaging data, clinical data, including MRI, sex, age

Exclusion criteria

  • Spinal cord concussion and MRI scans have no obvious positive performance of spinal cord
  • The quality of MRI images is insufficient or there are serious motion artifacts

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

China · 1 center
  • Affiliated 2 Hospital of Nantong University — Nantong

Identifiers

NCT: NCT06436716 · WuCS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗