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Recruiting NCT06099717

Clinical Performance of Dual-cantilevered Single-implant Bridge

Conditions: Dental Implant Failed

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: Yes
Phase: NA
Enrollment: 50
Sponsor: University of Bern

Location: Universidade Federal de Goias Goiânia Goiás

Summary

The study aims to evaluate the clinical performance (implant and prosthetic survival/ success rates) of a novel implant-supported fixed dental prosthesis design: the dual-cantilevered single implant bridge (T-Bridge) made out of monolithic zirconia bonded to a titanium base abutment (Variobase abutments)

Eligibility Criteria

Inclusion Criteria: * Age ≥ 20 years * Willingness to sign an informed consent and participate in the study * Three missing adjacent teeth in the posterior site. * Tooth gap of 21-24 mm. * Presence of natural or artificial opposing dentition * Sufficient vertical interocclusal space of an implant restoration (7mm) * Sufficient ridge height to place an implant of 10mm in length * Sufficient ridge width for the placement of a 4.1mm diameter implant. Simultaneous GBR to achieve a width of 6.5mm will be included. Exclusion Criteria: * Any physical or mental disorder that would interfere with the ability to perform adequate oral hygiene or the capability of providing written informed consent and compliance with the protocol * Any disorder that would interfere with wound healing or represent a contraindication for implant surgery, such as but not limited to uncontrolled diabetes or conditions resulting in or requiring immunosuppression, radiation, chemotherapy, frequent use of antibiotics or antiresorptive medication such as bisphosphonates. * Pregnancy or lactation * Heavy smoking habit with ≥ 10 cig/d * Severe bruxism or clenching habits, presence of oro-facial pain * Insufficient ridge width/height for the study implant

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06099717). StuddyBuddy aggregates publicly available trial information.