Tailored jaw implants put to the test for better smiles
NCT ID NCT05073757
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at how well custom-made implants work for people having jaw surgery (orthognathic surgery). 56 patients received personalized guides and plates during their operation. The main goal was to see if these implants improved patients' quality of life after surgery.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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56 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Feb 2025
- 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
Orthognatic surgery male or female patients, adults or minors whose bone maturity is sufficient according to the judgment of the investigator.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * Male or female patient, adult or minor having reached bone maturity according to the judgment of the investigator, * Patient having first orthognathic surgery with SLS France custom-made guides and plates, * Patient who received orthodontic treatment prior to orthognathic surgery, * Patient able to read, understand and answer the study quality of life questionnaire, * Patient (and legal representative if a minor) who is not opposed to his participation in the study or to the processing of his data. * Patient affiliated to a social insurance Exclusion Criteria: * Patient allergic to one of the compounds of the plates and / or guides, * Patient with physical or mental disability making it impossible to follow up in the study, * Patient with significant expansion * Patient with a congenital craniofacial malformation * Patient with acute or chronic local or systemic infection, * Person placed under legal protection, * Pregnant or breastfeeding women.
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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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Cabinet Orhognatic
Lyon, 69005, France
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Cabinet chirurgie Maxillo-faciale
Tournai, 7500, Belgium
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Hôpital Villefranche sur Sâone
Villefranche-sur-Saône, 69655, France
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Hôpital de la Loire
Saint-Etienne, 42100, France
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