New implants for facial fractures under review in 102-Patient study
NCT ID NCT05742932
First seen Jun 27, 2026 · Last updated Jul 08, 2026 · Updated 2 times
Summary
This study looks at how well and how safe Global D implants work for people who need surgery on their jaw or face after an injury. About 102 patients aged 11 and older will take part. The main goal is to see how well the jaw works 6 months after surgery using a simple questionnaire.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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99 people
The number who actually took part.
- Started
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Mar 2023
- Expected to finish
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Jul 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
The study population is composed of male and female, major or minor, who will be treated by trauma surgery. The patients will have maxillary, mandibular or maxillomandibular fractures with/without annex skull's or face's fractures.
- Ages
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11 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: * Male or female patient, major or minor (11 years old minimum) * Patient undergoing surgery on the mandible and/or maxilla (mandatory), with or without associated facial fractures (orbit, upper two-thirds of the face, skull) * Patient with abilities to read, understand and answer to the study questionnaires. * Patient (and his legal representative if minor) who signed the study consent form. * Patient affiliated to a social security system. Exclusion Criteria: * Patient allergic to one of the components of the implants * Patient with physical or mental inabilities that will compromise the follow-up during the study * Patient with acute or chronic infection (local or systemic) * Patients with bone's tumors in the anchorage area of the implant * Person on legal protection * Pregnant or breastfeeding women
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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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Hopital Femme Mère Enfant - Hospices Civils de Lyon (FRANCE)
Lyon, France
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Hopital de la Croix Rousse - Hospices Civils de Lyon (FRANCE)
Lyon, France
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Other studies related to the condition(s) this trial covers.
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