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Development and Clinical Validation of an Artificial Intelligence-Based Trauma Severity Assessment System

Development and Clinical Validation of an Artificial Intelligence-Based Trauma Severity Assessment System

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600118125
Enrollment
Unknown
Registered
2026-02-02
Start date
2026-02-02
Completion date
Unknown
Last updated
2026-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

trauma

Interventions

Gold Standard:Using the final trauma severity score assessed by clinical experts as the gold standard
Index test:Automated Trauma Severity Assessment System Based on Multimodal Artificial Intelligence

Sponsors

Army Center of Special Medical Service of PLA
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.During the period from January 1, 1997, to December 31, 2025, all trauma patients admitted to the emergency or trauma center of this hospital. 2.The primary diagnosis is a traumatic disease (according to the International Classification of Diseases, ICD-10 codes, such as the S00-T98 series), and trauma is the main reason for this visit. 3.Complete initial vital signs records are available (including at least heart rate, blood pressure, respiratory rate, body temperature, and Glasgow Coma Scale score). Analyzable imaging data (such as CT scans, X-rays) or complete structured imaging reports are available. Core laboratory test results (such as complete blood count, blood gas analysis, coagulation function, and blood lactate) are available.

Exclusion criteria

Exclusion criteria: 1.All records for any of the key data categories specified in inclusion criterion 3 above (vital signs, imaging, laboratory) are missing. 2.Patients with non-traumatic emergencies (such as acute myocardial infarction, stroke, poisoning) or acute exacerbations of chronic diseases. 3.Patients with delayed presentation, defined as those whose time from injury to first medical contact exceeds 72 hours.

Design outcomes

Primary

MeasureTime frame
Consistency of AI System and Gold Standard in Grading Trauma Severity;Accuracy;Area under the receiver operating characteristic curve;

Countries

China

Contacts

Public ContactChengyi Wu

Army Center of Special Medical Service of PLA

1945867241@qq.com+86 23 6872 9230

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026