Implant-supported Fixed Dental Prostheses (FDPs) With Cantilever Extension
NCT ID: NCT05676268
Last Updated: 2026-01-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
35 participants
OBSERVATIONAL
2023-01-02
2023-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients with oral implants supporting full ceramic fixed dental prostheses
Implant-supported fixed dental prostheses with cantilever extension
Healthy patients in need of replacement of missing teeth with dental implants supporting partial fixed dental prostheses with cantilever extensions
Interventions
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Implant-supported fixed dental prostheses with cantilever extension
Healthy patients in need of replacement of missing teeth with dental implants supporting partial fixed dental prostheses with cantilever extensions
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
99 Years
ALL
Yes
Sponsors
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University of Bern
OTHER
Responsible Party
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Principal Investigators
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Andrea Roccuzzo
Role: PRINCIPAL_INVESTIGATOR
University of Bern
Locations
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Department of Periodontology, University of Bern
Bern, , Switzerland
Countries
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Other Identifiers
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FDPs with cantilever
Identifier Type: -
Identifier Source: org_study_id
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