Actively Recruiting
Artificial Intelligence Model for Traumatic Cervical Spinal Cord Injury Based on Radiomics and Genomics to Build a Clinical Data Platform
Led by Affiliated 2 Hospital of Nantong University · Updated on 2024-05-31
300
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting detailed and standardized information about traumatic cervical spinal cord injuries to create a high-quality clinical data platform. This platform aims to support analysis and research by providing a shared database of spinal cord injury cases, promoting collaboration across multiple centers, and enhancing the competitiveness of spinal cord injury research internationally. The project also seeks to help regional hospitals establish a connected network for data sharing on spinal cord injuries. The study includes groups with no spinal cord injury (control) and spinal cord injury patients classified by the American Spinal Injury Association (ASIA) grades A through D. Every patient undergoes MRI scans, which are essential for assessing the spinal cord injury. The data collected includes MRI images, clinical information, and demographic details such as age, gender, weight, height, and body mass index (BMI). Data collection spans from 2016 through 2027. Participants will have imaging and clinical assessments including MRI scans within 48 hours after injury, with ongoing collection of ASIA scores to evaluate injury severity. Researchers will monitor outcomes such as MRI findings and ASIA scores over the study period. Secondary measures like age, gender, weight, height, and BMI are also recorded. The study is observational and open to healthy volunteers, supporting long-term data gathering to improve spinal cord injury research and care.
CONDITIONS
Brief Title
Artificial Intelligence Model for Traumatic Cervical Spinal Cord Injury Based on Radiomics and Genomics
Who Can Participate
Eligibility Criteria
You may qualify if you...
- MRI diagnosis of traumatic cervical spinal cord injury (TCSCI)
- Clinical diagnosis of TCSCI
- Injury site must be in the cervical spinal cord
- MRI images of T2-weighted imaging collected within 48 hours after injury
- Complete and available imaging and clinical data including MRI, sex, and age
You will not qualify if you...
- Spinal cord concussion without clear positive MRI findings
- Insufficient MRI image quality or serious motion artifacts in MRI scans
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Data collection from 2016 to 2027
Participants undergo MRI scans and clinical assessments to gather imaging and clinical data related to traumatic cervical spinal cord injury.
MRI performed within 48 hours after injury; additional assessments may occur depending on clinical status
Duration - From 2016 to 2027
Participants are observed over time to monitor MRI images and ASIA scores along with demographic and clinical data.
Ongoing data collection during the study period
Trial Site Locations
Total: 1 location
1
Affiliated 2 Hospital of Nantong University
Nantong, Jiangsu, China, 0513
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
4
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