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Recruiting NCT06436716

NCT06436716 Artificial Intelligence Model for Traumatic Cervical Spinal Cord Injury Based on Radiomics and Genomics

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Clinical Trial Summary
NCT ID NCT06436716
Status Recruiting
Phase —
Sponsor Affiliated 2 Hospital of Nantong University
Condition Spinal Cord Injuries
Study Type OBSERVATIONAL
Enrollment 300 participants
Start Date 2016-01
Primary Completion 2026-12

Eligibility & Interventions

Sex All sexes
Min Age N/A
Max Age N/A
Study Type OBSERVATIONAL
Interventions
MRI

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 300 participants in total. It began in 2016-01 with a primary completion date of 2026-12.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: 1. MRI Diagnosis of TCSCI 2. Clinic Diagnosis of TCSCI 3. The injury site must be in cervical spinal cord 4. MRI images of T2WI must be collected within 48 hours after injury 5. Complete and available imaging data, clinical data, including MRI, sex, age Exclusion Criteria: 1. Spinal cord concussion and MRI scans have no obvious positive performance of spinal cord 2. The quality of MRI images is insufficient or there are serious motion artifacts

Frequently Asked Questions

Who can join the NCT06436716 clinical trial?

This trial is open to participants of all sexes, studying Spinal Cord Injuries. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06436716 currently recruiting?

Yes, NCT06436716 is actively recruiting participants. Visit ClinicalTrials.gov or contact Affiliated 2 Hospital of Nantong University to inquire about joining.

Where is the NCT06436716 trial being conducted?

This trial is being conducted at Nantong, China.

Who is sponsoring the NCT06436716 clinical trial?

NCT06436716 is sponsored by Affiliated 2 Hospital of Nantong University. The trial plans to enroll 300 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology