跳至主要内容
临床试验/NCT06754137
NCT06754137
招募中
不适用

Evaluating the Cost-Efficiency and Workflow Impact of AI-Supported Fracture Detection in an Orthopedic Emergency Care Unit

Salzburger Landeskliniken3 个研究点 分布在 2 个国家目标入组 4,800 人2025年3月31日

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Fractures, Bone
发起方
Salzburger Landeskliniken
入组人数
4800
试验地点
3
主要终点
Diagnostic Accuracy of Fracture Detection
状态
招募中
最后更新
3个月前

概览

简要总结

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.

详细描述

This clinical trial aims to evaluate the cost-efficiency and workflow impact of AI-assisted fracture detection in an orthopedic emergency care unit. The study is designed as a prospective, randomized, controlled trial to assess whether integrating AI technology can improve diagnostic accuracy, streamline workflow, and reduce healthcare costs compared to the traditional diagnostic approach. Study Objectives Primary Objectives: The primary objective of the SMART Fracture Trial is to assess the impact of AI-assisted X-ray interpretation on physician decision-making and clinical workflows. The study will therefore provide deeper insights into AI's potential benefits and limitations beyond theoretical performance metrics. Secondary Objectives: While the primary focus of the SMART Fracture Trial is on AI's clinical integration, the study will also comprehensively assess diagnostic accuracy and classification performance - key factors that influence real-world implementation. By analyzing these secondary objectives, the study will provide deeper insights into AI's theoretical performance metrics. Study Design This is a prospective, randomized, controlled trial conducted as an international multi-center study. It includes two parallel arms: Control Group: Standard diagnostic procedures without AI assistance. Intervention Group: AI-based diagnostic tools assist in interpreting radiological images. Both groups will follow the same diagnostic imaging protocol, including standard X-ray imaging in two planes. The AI software, pre-validated for fracture detection, will be integrated into the hospital's Picture Archiving and Communication System (PACS). Intervention Details The AI fracture detection systems (Aidoc, Gleamer) are designed to identify fracture patterns, bone lesions, effusion and dislocations on X-rays and highlight areas of potential concern for physician review. The software operates in real time, providing marked-up images to physicians. The AI output serves as a diagnostic aid, with final diagnoses made by the attending physician. Population and Sampling Population: Patients of all ages presenting to the emergency care unit with isolated extremity injuries or isolated joint complaints. Sample Size: Approximately 4,800 participants (2400 per group) to ensure sufficient statistical power for primary outcomes. Randomization: Participants will be randomly assigned to the control or intervention group using a 1:1 allocation ratio. Outcome Measures Primary Outcome Measures: Diagnostic accuracy: Sensitivity, specificity, and AUC of AI-assisted vs. traditional diagnosis. Time to diagnosis: Total time from patient triage to final diagnosis. Secondary Outcome Measures: Cost analysis: A detailed cost comparison of the diagnostic process in both groups. Diagnostic confidence: Assessed using a Likert scale (1-10) completed by physicians after reviewing each case. Study Procedures Baseline Data Collection: Demographics, clinical history, and presenting symptoms will be recorded at enrollment. Standard radiological imaging will be conducted for all participants. AI Integration (Intervention Group): Radiological images will be processed by AI software, providing annotated images to physicians. AI-assisted diagnostic workflows will be compared to standard workflows. Outcome Assessment: All diagnoses will be independently reviewed by a panel of experts, including an experienced radiologist and orthopedic surgeon, to establish a reference standard for comparison. Ethical Considerations The study adheres to the principles of the Declaration of Helsinki and has received approval from the local ethics committee. Written informed consent will be obtained from all participants before enrollment. Data will be pseudonymized to maintain confidentiality. Expected Impact This study aims to provide robust evidence regarding the effectiveness of AI in improving diagnostic workflows in emergency care settings. Findings may inform the future integration of AI tools into clinical practice, improving patient outcomes and optimizing resource utilization in high-volume emergency care environments.

注册库
clinicaltrials.gov
开始日期
2025年3月31日
结束日期
2026年4月30日
最后更新
3个月前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

发起方
Salzburger Landeskliniken
责任方
Principal Investigator
主要研究者

Martin Breitwieser

Principal Investigator

Salzburger Landeskliniken

入排标准

入选标准

  • Presenting to the emergency department with an isolated injury or joint complaint
  • Patients able and willing to provide informed consent.

排除标准

  • 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.

结局指标

主要结局

Diagnostic Accuracy of Fracture Detection

时间窗: At the time of initial diagnosis, within 2 hours of patient presentation to the orthopedic emergency unit

The primary outcome measures the diagnostic accuracy of detecting fractures using sensitivity, specificity, and the area under the receiver operating characteristic curve (AUC). Diagnostic accuracy will be compared between the AI-assisted diagnostic approach and the standard physician-only approach. The gold standard for comparison will be determined by expert consensus based on independent review by a radiologist and an orthopedic specialist.

次要结局

  • Time to Diagnosis(During the patient's emergency department visit, typically within 4 hours of presentation.)
  • Physician Diagnostic Confidence(Measured immediately after the diagnosis)
  • Cost-Efficiency of Diagnostic Workflow(Calculated at the end of the study for all enrolled participants, approximately 6 months from study initiation.)

研究点 (3)

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