Proximal Femur Image Database Validation

April 4, 2024 updated by: AO Innovation Translation Center

Validation of the Fracture Classification Accuracy (Ground Truth) of Anteroposterior X-ray of the Proximal Femur According to the Arbeitsgemeinschaft für Osteosynthesefragen/Orthopedic Trauma Association Classification Done by a Single Center: A Pilot Validation Study

The AO@AI Turin project is a collaborative project with a Turin group and the AO (Arbeitsgemeinschaft für Osteosynthesefragen, or in English, Association for the Study of Internal Fixation) foundation. An Image database (DB) has been built to host AP pelvic radiographs ready for artificial intelligence (AI) development.

The goal of this project is to determine the agreement between the Turin annotation of fracture status and the annotation from an external group of AO expert surgeons for a random subset of the Turin images.

Study Overview

Detailed Description

The AO@AI Turin project is a collaborative project with a Turin group who has collected 2,932 anteroposterior (AP) pelvic radiographs, of which 1,811 are fracture images, and 1,121 are non-fracture images. The Turin group has developed an artificial intelligence (AI) algorithm for fracture classification using these images. These anonymized images (with all metadata or personal identifiers removed) have been uploaded to a cloud-based image database (DB) hosted and managed by the AO Foundation.

The Turin group has established the "ground truth" using the methods of "consensus by experts". Two radiologists from their medical team have reviewed and classified the fracture status (fracture vs non-fracture, and, if fracture, the AO/Orthopedic Trauma Association [OTA] classification).

The next step's goal is the ground truth validation plan to test the accuracy of the Turin annotation of fracture classification of the already uploaded AP pelvic images. This is to ensure that the image DB offers accurate quality annotations to allow AI development.

For the pilot phase, a random subset of the Turin images (300 of images) will be drawn from the image DB. These images will be reviewed by an external group of AO expert surgeons who will annotate the images per their fracture status, i.e., fracture vs non-fracture, and, if fracture, the AO/OTA classification.

The group of AO expert surgeons consists of four surgeons who will independently review the 300 images and a fifth surgeon who serves as an adjudicator if necessary. The expert surgeons will be given access to the 300 images via the cloud-based image DB and annotate the images. The expert surgeons will be blinded to the Turin annotations. The expert surgeons' annotations will be entered into a DB built for the purpose for the pilot study.

To determine the ground truth, the annotations of the four surgeons will be compared, and discrepancies will be identified. A meeting will then be arranged among the surgeons to resolve, by consensus, the discrepancies, with the potential involvement of the fifth surgeon as the adjudicator. After the resolution meeting, there will be a single set of annotations for the 300 images from the exert surgeon group.

The Turin annotations will also be entered into the study DB to allow comparisons with the expert surgeon group's annotation.

In case of disagreement between the Turin annotation and the AO expert surgeon annotations, a consensus will be sought to establish a new ground truth. If this process results in significant revisions to the annotations, the entire dataset will be reviewed to set this new standard. Following such a comprehensive dataset revision, the algorithm for automated fracture classification of the proximal femur, which has already been developed by the Turin group, will be re-trained. After re-training, the algorithm's performance will be evaluated through metrics such as precision, recall, and F1-score to ensure its accuracy and effectiveness in classifying proximal femur fractures.

Study Type

Observational

Enrollment (Estimated)

2932

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Dübendorf, Switzerland, 8600
        • AO foundation

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Anonymized anteroposterior x-ray images in the Image database (DB). No patients will be enrolled for purposes of this study. The selection of 300 images for the pilot validation is random; therefore, the sampling method indicated below refers to this process of random selection of images from the Image DB.

Description

Inclusion criteria

  • Not applicable.
  • The study utilizes the anonymized images in the Image database (DB). No patients will be enrolled for purposes of this study.

Exclusion criteria

• Not applicable.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Annotations of fracture status of the image
Time Frame: Day 0/Baseline
Fracture status (fracture vs no fracture) classification
Day 0/Baseline
In case of fracture, Arbeitsgemeinschaft für Osteosynthesefragen (AO, in English, Association for the Study of Internal Fixation)/Orthopedic Trauma Association (OTA) classification: Type
Time Frame: Day 0/Baseline
AO/OTA classification: Type: 31A/31B/31C
Day 0/Baseline
In case of fracture, AO/OTA classification: Group
Time Frame: Day 0/Baseline
AO/OTA classification: Group: A1/A2/A3, B1/B2//B3, C1/C2
Day 0/Baseline
In case of fracture, AO/OTA classification: Subgroup
Time Frame: Day 0/Baseline
AO/OTA classification: Subgroup: A1.1/A1.2/A1.3/A2.2/A2.3/A3.1/A3.2/A3.3/B1.1/B1.2/B1.3/B2.1/B2.2/B2.3/C1.1/C1.2/C1.3/C2.1/C2.2/C2.3
Day 0/Baseline
In case of fracture, AO/OTA classification: Qualifier for 31A1.1
Time Frame: Day 0/Baseline
AO/OTA classification: Qualifier for 31A1.1: n/o
Day 0/Baseline
In case of fracture, AO/OTA classification: Qualifier for 31B2
Time Frame: Day 0/Baseline
AO/OTA classification: Qualifier for 31B2: p/q/r
Day 0/Baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Alessandro Aprato, MD, University of Turin, Italy

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2021

Primary Completion (Estimated)

October 1, 2024

Study Completion (Estimated)

June 30, 2025

Study Registration Dates

First Submitted

March 26, 2024

First Submitted That Met QC Criteria

April 4, 2024

First Posted (Actual)

April 8, 2024

Study Record Updates

Last Update Posted (Actual)

April 8, 2024

Last Update Submitted That Met QC Criteria

April 4, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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