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Standing x-rays may reveal what lying scans miss in shoulder replacement planning
NCT ID NCT07819149
First seen Sep 14, 2026 · Last updated Sep 18, 2026 · Updated 3 times
Summary
People scheduled for total shoulder replacement often get a CT scan while lying on their back to measure how far the upper arm bone slips backward. Researchers want to know whether that measurement changes when a person stands. The trial uses a low-dose biplanar X-ray booth called EOS to scan participants in both positions and compare the results. About 92 adults scheduled for shoulder replacement take part.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- biplanar fluoroscopy EOS imaging, a low-dose standing X-ray scan
- What this could lead to
- If standing scans give a clearer picture of the shoulder than lying scans, surgeons could plan shoulder replacements using measurements that better match how people actually move.
- What could go wrong
- This is a small imaging study, not a treatment trial. It may show that standing and lying scans agree, or the findings may not change how surgeons choose or place implants.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 92 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Major * Scheduled for shoulder arthroplasty * Having undergone a CT scan of the shoulder scheduled for arthroplasty prior to the operation * Patient having signed an informed consent form * Patient affiliated with a social security scheme or beneficiary of such a scheme, according to Article L.1124-1 of the Public Health Code Exclusion Criteria: * Contraindications from surgeons * Contraindication to EOS® examination * Anthropometry incompatible with EOS® examination * Scheduled for shoulder arthroplasty due to : fracture, sequelae of a fracture, history of glenoid graft * History of fracture of the humerus, scapula, or clavicle * Vulnerable and/or protected individual: adult under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative decision * Pregnant, breastfeeding, or postpartum woman
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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
1 site. 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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Hôpital privé Jean Mermoz
Lyon, 69008, France
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