AI could spot brittle bones from routine chest X-Rays
NCT ID NCT07421713
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests an artificial intelligence software called Osteo Signal that analyzes chest X-rays to detect signs of osteoporosis or osteopenia in adults aged 50 and older. Researchers will compare the AI's accuracy against the standard DXA bone density scan using data from 595 people who already had both exams. If it works, this could make osteoporosis screening faster and more accessible without extra tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Osteo Signal (AI software)
- What this could lead to
- If successful, this could provide a quick, low-cost way to screen for osteoporosis using routine chest X-rays, without extra radiation or visits.
- What could go wrong
- This is a retrospective study using existing data, not a real-world test. The AI may not work as well in different hospitals or populations, and it only screens for risk, not a diagnosis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 595 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Mar 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients selected hospitals in the Netherlands and UK that have previously had chest x-rays and DXA scans
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age ≥50 years at the time of chest X-ray 2. Availability of 1. Posteroanterior (PA) Chest X-ray and 2. DXA scan with a valid T-score measurement where both the DXA scan and Chest x-ray examinations were performed within 6 months (182 days) of each other and 3. Available X-ray and DXA scans performed on or after 01-Jan-2010. 3. Complete metadata (sex and age) available on PACS or hospital records. Exclusion Criteria: 1. Non-diagnostic Quality or Incomplete Imaging of: 1. DXA scan inadequacy: Missing T-score from a technically inadequate scan. 2. PA Chest X-ray technical inadequacy: Non-PA projection, significant motion artefacts, inadequate visualisation of thoracic structures, or missing DICOM metadata. 3. Image format incompatibility: Non-DICOM format or corrupted image files that would prevent AI analysis 4. PA Chest X-ray \> ±6 months from the date of the DXA scan. 2. Previous diagnosis or treatment of Osteoporosis prior to the DXA scan used in the Study. 1. diagnosis of osteoporosis (T-score ≤-2.5), or current/recent anti- osteoporotic medications, within 12 months prior to the DXA scan used in the study. 2. Current or recent anti-osteoporotic medications for 3 months (91 days) continuously prior to the Chest x-ray used in the Study. 3. Diagnosis of any metabolic bone disease prior to the DXA scan used in the study. 4. Diagnosis of metabolic bone disease other than Osteoporosis or Osteopenia, up to a maximum of 3 months (91 days) after the DXA scan. 5. Major Chest Wall or Spinal Deformities, including but not limited to: 1. Severe structural deformities: Thoracic scoliosis with Cobb angle \>40°, severe kyphosis, or chest wall deformities (pectus excavatum/carinatum) affecting \>30% of the thoracic cage. 2. Surgical hardware: Previous thoracic/spinal surgery with metallic implants obscuring anatomical landmarks required for AI analysis. 3. Pathological conditions: Extensive pulmonary consolidation, pleural effusion, lesions or masses obscuring \>30% of thoracic skeletal structures 6. Subject has opted out of confidential data being used for research purposes
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Barts Health NHS Trust
RECRUITINGLondon, E1 4DG, United Kingdom
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Erasmus University Medical Center Rotterdam,
NOT_YET_RECRUITINGRotterdam, 3015 GD, Netherlands
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Mid and South Essex NHS Foundation Trust
NOT_YET_RECRUITINGWestcliff-on-Sea, Essex, SS0 0RY, United Kingdom
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