Shoulder device under 10-Year watch
NCT ID NCT03423953
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 194 people who received the Comprehensive Nano shoulder device to replace their shoulder joint due to arthritis, bone death, or deformity. Researchers will track how long the implant lasts and how well patients can use their shoulder over 10 years. The goal is to gather real-world data on safety and performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Comprehensive Nano shoulder device
- What this could lead to
- If successful, this could confirm the device's long-term safety and effectiveness for shoulder replacement.
- What could go wrong
- This is an observational post-market study, not a controlled trial, so results may not prove the device is better than alternatives. Risks include typical surgery complications like infection or implant failure.
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 194 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2013
- Expected to finish
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Jul 2030
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 in need of an uncemented shoulder arthroplasty and who meet all of the inclusion and none of the exclusion criteria.
- Ages
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18 years and older
- Sex
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Anyone
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: * Non-inflammatory degenerative joint disease including osteoarthritis and avascular necrosis. * Rheumatoid arthritis * Revision where other devices or treatments have failed * Correction of functional deformity. * Difficult clinical management problems where other methods of treatment may not be suitable or may be inadequate * Difficult clinical management problems where other methods of treatment may not be suitable or may be inadequate Exclusion Criteria: * Infection * Sepsis * osteomyelitis
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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.
Contacts and locations
Locations
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Chonnam National University Hospital
Gwangju, Gwangju, South Korea
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Kingston General Hospital
Kingston, Ontario, K7L 3N6, Canada
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Privatklinik Leech
Graz, Styria, 8010, Austria
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Samsung Medical Centre
Seoul, Seoul, 06351, South Korea
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University of Liverpool
Liverpool, Merseyside, L69 3BX, United Kingdom
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