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Trauma (Including Fractures)AI-TraumatNCT07329881

Artificial Intelligence Algorithm for the Interpretation of Traumatic Bone Radiographs

An observational study of Trauma (Including Fractures), run by Hôpital Universitaire Sahloul at 1 site in Tunisia.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This diagnostic study aims to compare the performance of an artificial intelligence (AI) algorithm designed to assist in the interpretation of traumatic bone radiographs (all anatomical regions excluding the thorax) with that of human readers, including emergency medicine and family medicine residents as well as… Read more about this study

Who is it for?
Any age
Conditions the study is for
Trauma (Including Fractures)
How many people
500 participants
Where
1 siteTunisia
Study dates
1 Nov 2025to 31 Mar 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Study Population and Eligibility Criteria Inclusion Criteria: Standard radiographs performed for suspected bone trauma (upper limbs, lower limbs, pelvis/hip, cervical/thoracolumbar spine) in the emergency setting. Adult and pediatric patients (informed consent by patient or legal guardian for minors). Acute trauma context. Exclusion Criteria: Poor-quality images (motion artifact, underexposure preventing diagnostic interpretation). Cases lacking senior interpretation for gold standard reference. Patients referred with radiographs performed outside the hospital (external facilities).

Who may be able to join

  • Standard radiographs performed for suspected bone trauma (upper limbs, lower limbs, pelvis/hip, cervical/thoracolumbar spine) in the emergency setting.
  • Adult and pediatric patients (informed consent by patient or legal guardian for minors).
  • Acute trauma context.

Who cannot join

  • Poor-quality images (motion artifact, underexposure preventing diagnostic interpretation).
  • Cases lacking senior interpretation for gold standard reference.
  • Patients referred with radiographs performed outside the hospital (external facilities).

Trial locations and contacts

1 site in 1 country.

Tunisia1 site
  • CHU sahloul

    Sousse

Other trials in Tunisia

About this study

Official title: Comparative Evaluation of the Performance of an Artificial Intelligence Algorithm for the Interpretation of Traumatic Bone Radiographs

This diagnostic study aims to compare the performance of an artificial intelligence (AI) algorithm designed to assist in the interpretation of traumatic bone radiographs (all anatomical regions excluding the thorax) with that of human readers, including emergency medicine and family medicine residents as well as senior physicians (one emergency medicine specialist and one orthopedic surgeon).

The study follows a paired reader study design: identical anonymized radiographic images are independently interpreted by the AI system and by human readers. The reference standard ("gold standard") will be defined by the consensus reading of the two senior physicians. Inter-observer agreement (kappa statistics) between the AI, residents, and senior reference readings will be estimated, and false negatives and false positives will be analyzed by lesion type and anatomical location.

Read the detailed description

This diagnostic accuracy study is designed to evaluate and compare the performance of an artificial intelligence (AI) algorithm with that of human readers in the interpretation of traumatic bone radiographs. The study focuses on radiographs of all skeletal anatomical regions except the thorax (e.g., skull, upper limbs, pelvis, and lower limbs) obtained in the context of acute trauma.

Study Design

The investigation will employ a paired reader design, meaning that each radiographic image will be interpreted independently by both the AI system and multiple human readers. This design allows direct, within-case comparison of diagnostic performance between the AI algorithm and human interpreters, minimizing variability related to case mix.

Study Population and Image Selection

Radiographs will be retrospectively collected from the hospital's Picture Archiving and Communication System (PACS). Eligible cases will include all conventional radiographs performed for suspected bone trauma over a defined inclusion period. Images must meet adequate technical quality standards and contain no patient-identifiable information. Exclusion criteria include incomplete imaging studies, thoracic images, and cases lacking definitive follow-up or diagnostic confirmation.

Image Preparation and Anonymization

All selected radiographs will be anonymized and assigned a random identification code. The dataset will be organized by anatomical region and then randomized to prevent recognition bias among readers.

Readers and Reading Procedure

Interpretations will be performed by:

Artificial Intelligence (AI) system: A deep learning algorithm trained to detect bone fractures and other traumatic findings on plain radiographs.

Human readers:

Two groups of resident physicians (emergency medicine and family medicine residents) with varying levels of training.

Two senior physicians, one emergency medicine specialist and one orthopedic surgeon, who will serve as expert readers.

Each image will be read independently by the AI algorithm and by each human reader, without access to clinical information or to the interpretations of others.

Reference Standard (Gold Standard)

The reference standard diagnosis for each radiograph will be established through a consensus review by the two senior physicians. In cases of initial disagreement, consensus will be reached through joint discussion, with review of clinical or additional imaging data if necessary.

Outcome Measures

The primary outcome measure will be the diagnostic accuracy of the AI algorithm compared with human readers for detecting bone fractures and other traumatic lesions, using the expert consensus as the gold standard.

Secondary Outcomes

Inter-observer agreement between the AI system and each human reader will be quantified using Cohen's kappa (κ) statistics.

Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) will be calculated for all readers and the AI.

Error analysis will be performed to characterize false negatives and false positives according to lesion type (e.g., cortical break, avulsion, dislocation) and anatomical location (e.g., wrist, ankle, pelvis).

Subgroup analyses will assess differences in performance by anatomical region and by reader experience level.

Statistical Analysis

Continuous variables will be expressed as means ± standard deviation or medians with interquartile ranges. Categorical data will be summarized as frequencies and percentages. Diagnostic performance metrics will be compared using appropriate statistical tests (e.g., McNemar's test for paired proportions). Confidence intervals (95%) will be calculated for all main estimates. A p-value < 0.05 will be considered statistically significant.

Ethical Considerations

The study will be conducted in accordance with institutional and ethical guidelines for retrospective diagnostic research. Since all radiographs will be anonymized and analyzed retrospectively, informed consent requirements may be waived by the ethics committee.

Keywords
IA, Validation, Trauma
Medical subject headings
Wounds and Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07329881
Study groupRoleWhat they receive
Residents (human readers)Residents (human readers)
Artificial Intelligence (AI) algorithmArtificial Intelligence (AI) algorithm

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Diagnostic sensitivity and specificity of the AI algorithm compared to human readers

    Sensitivity and specificity for detection of traumatic bone lesions on radiographs, using the senior physicians' consensus reading as the reference standard (gold standard).

    Measured: At the end of image interpretation for each reader (expected within 1 month after image collection).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Jan 2026
  2. Study start1 Nov 2025
  3. Primary completion30 Mar 2026 (estimated)
  4. Study completion31 Mar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
500 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07329881
Sponsor's protocol ID
AI-Traumat
Acronym
AI-Traumat
Status last verified
Nov 2025
First submitted
29 Dec 2025
Last updated
9 Jan 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Trauma (Including Fractures), run by Hôpital Universitaire Sahloul at 1 site in Tunisia.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 9 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Tunisia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Diagnostic sensitivity and specificity of the AI algorithm compared to human readers (time frame: At the end of image interpretation for each reader (expected within 1 month after image collection).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Jan 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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