New dental implant design shows promise in small study
NCT ID NCT05676268
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested how well dental implants with ceramic extensions (cantilevers) work after at least 1 year. Researchers followed 35 healthy adults who needed replacement teeth. They checked implant survival, bone changes, and any complications. The goal was to see if this approach is reliable for everyday use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could provide evidence that ceramic cantilever extensions on dental implants are a reliable option for replacing missing teeth.
- What could go wrong
- This is a small, early proof-of-principle study with only 35 participants and a short follow-up of 1 year. Results may not apply to everyone, and long-term success is unknown.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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35 people
The number who actually took part.
- Started
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Jan 2023
- Finished
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Dec 2023
- 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.
Who is studied
Patients with missing teeth rehabilitated with dental implants supporting partial fixed dental prostheses with cantilever extensions
- Ages
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18 to 99 years
- 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: * Patients aged ≥18 years * Written informed consent * Patients with systemic health or controlled medical conditions * Patients with healthy or treated periodontal conditions * Patients enrolled in regular supportive periodontal therapy (SPT) * Patients without clinical signs of bruxism and/or oral parafunctions * 2 osseointegrated dental implants in the canine or posterior areas of maxilla and mandible following transmucosal placement and healing of 3-6 months * Tissue level solid-screw implants with a sand-blasted and acid- etched (SLA) surface with an endosseous diameter of 3.3, 4.1 or 4.8 mm, a length of 8, 10 or 12 mm, a shoulder diameter of 4.8 mm and a supracrestal machined neck with a height of 1.8 or 2.8 mm (Straumann® Dental Implant System, Institut Straumann AG, Basel, Switzerland) * Full-ceramic * Utilization of prefabricated titanium abutments * Cemented (3M™ ESPE Ketac™ Cem, Seefeld, Germany) or screw-retained fixed dental prostheses with a mesial or distal cantilever extension (FDPCs) * Cantilever extension corresponding to 1 premolar unit (i.e., 6-7 mm) * Absence of occlusal contacts or guidance on the cantilever extension at baseline * Opposing dentition consisting of natural teeth or fixed or removable prosthetic restorations * Availability of a periapical radiograph at baseline (i.e. FDPC delivery) * Availability of PPD measurements (mm) taken at baseline at 4 sites/implant with a graduated Michigan periodontal probe (Deppeler SA, Rolle, Switzerland) * Availability of BoP measurements (%) (Lang et al., 1986) taken at baseline at 4 sites/implant with a graduated Michigan periodontal probe (Deppeler SA, Rolle, Switzerland). Exclusion Criteria: * Untreated or active periodontal diseases * Immediate implant placement (i.e., Type I implant placement according to Hämmerle et al., 2004) * FDPCs in the aesthetic zone (i.e., replacement of maxillary or mandibular incisors) * FDPCs supported by hollow-screw and hollow-cylinder implants
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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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Department of Periodontology, University of Bern
Bern, 3010, Switzerland
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Other studies related to the condition(s) this trial covers.
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