← Back to Clinical Trials
Recruiting NCT06754137

Assessing AI-Supported Fracture Detection in Emergency Care Units

◆ AI Clinical Summary
Plain-language summary for patients

Trial Parameters

Condition Fractures, Bone
Sponsor Salzburger Landeskliniken
Study Type INTERVENTIONAL
Phase N/A
Enrollment 4,800
Sex ALL
Min Age N/A
Max Age N/A
Start Date 2025-03-31
Completion 2026-04-30
Interventions
AI-Assisted Fracture Detection SystemStandard Physician-Interpreted Fracture Detection

Eligibility Fast-Check

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

Brief Summary

Brief Summary The purpose of this study is to determine if artificial intelligence (AI) can assist doctors in detecting broken bones, effusions, dislocations and bone lesions more quickly and accurately in an emergency room setting. The study will also evaluate whether AI can save time and reduce costs in healthcare. The main questions to be addressed are: * Does AI improve the accuracy of detecting broken bones/dislocations/effusions/bone lesions? * Can AI expedite the process of diagnosing broken bones/dislocations/effusions/bone lesions? * Does AI reduce healthcare costs by enhancing efficiency? To investigate these questions, two groups of patients will be compared. One group will follow the traditional diagnostic approach, while the other group will utilize AI to assist in diagnosing X-rays. Participants in the study will: Undergo standard X-ray imaging of injured arms or legs, as part of routine care. Have X-rays reviewed by doctors with or without AI support, depending on the assigned group. The study will include patients of all ages presenting to the emergency room with an isolated injury or joint complaints. No additional tests or treatments beyond standard care will be involved.

Eligibility Criteria

Inclusion Criteria: * Presenting to the emergency department with an isolated injury or joint complaint * Patients able and willing to provide informed consent. Exclusion Criteria: * Patients with injuries or complaints involving multiple body regions * Patients with prior imaging of the affected extremity or region within the past 6 months * Contraindications to X-ray imaging (e.g., pregnancy or severe instability) * Patients with other ongoing studies that may interfere with this study * Patients unable to provide consent due to cognitive impairment or language barriers without an available representative.

Related Trials

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: April 2026  ·  Data Methodology
}