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Survival of Titanium-Zirconium and Titanium Dental Implants in Cigarette-smokers and Never-smokers: A 5-Year Follow-up.

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To compare the peri-implant clinical and radiographic status around bone-level narrow-diameter titanium-zirconium (TiZr) implants and titanium (Ti) implants placed in cigarette-smokers (CS) and never-smokers (NS).Partially edentulous CS and NS rehabilitated

Zirconium dioxide implant abutments for posterior single-tooth replacement: first results.

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BACKGROUND Prefabricated implant abutments made of zirconium dioxide (yttria-stabilized polycrystalline tetragonal zirconia; Y-TZP) have proved to be useful in the esthetically demanding anterior region and may also be useful for premolar and molar replacement because of their obvious positive

All-Ceramic Zirconium Dioxide Implant Abutments for Single-Tooth Replacement in the Posterior Region: A 5-Year Outcome Report.

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To assess the clinical performance of a prefabricated all-ceramic zirconium dioxide implant abutment for single-tooth replacement in the posterior region.Forty implants (Xive S plus screw type, Dentsply Sirona Implants) were inserted into the posterior

Success and survival rates of narrow diameter implants made of titanium-zirconium alloy in the posterior region of the jaws - results from a 1-year follow-up.

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OBJECTIVE The aim of the present prospective clinical study was to evaluate and to compare the success and survival rates of narrow diameter implants made of titanium-zirconium alloy and commercially pure titanium. METHODS Forty-two healthy adult patients scheduled for implant-supported single

Prefabricated zirconium dioxide implant abutments for single-tooth replacement in the posterior region: evaluation of peri-implant tissues and superstructures after 12 months of function.

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OBJECTIVE In the present study, prefabricated abutments made of zirconium dioxide Y-TZP (tetragonal zirconia polycrystals) were inserted into the posterior region under controlled clinical conditions. The aim was to test whether abutments made of zirconium dioxide are suitable for this indication.

Pre-fabricated zirconium dioxide implant abutments for single-tooth replacement in the posterior region: success and failure after 3 years of function.

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OBJECTIVE Zirconia implant abutments have gained a much broader clinical use over the past few years. The aim of the present study was to assess the clinical performance of a pre-fabricated zirconium dioxide implant abutment for single-tooth replacement in the posterior region. METHODS Forty

The Novel Design of Zirconium Oxide-Based Screw-Retained Restorations, Maximizing Exposure of Zirconia to Soft Peri-implant Tissues: Clinical Report After 3 Years of Follow-up.

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Current use of zirconium oxide (ZrO₂)-based screw-retained restorations does not guarantee maximum contact of soft peri-implant tissues with ZrO₂, because veneering porcelain usually covers the major subgingival part of the restoration. Ceramics preclude direct interaction between zirconia and soft

Three-year split-mouth randomized clinical comparison between crowns fabricated in a titanium-zirconium and a gold-palladium alloy.

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OBJECTIVE The aim of this study was to compare the clinical performance of metal-ceramic crowns made with an experimental alloy prepared by the Nordic Institute of Dental Materials, containing 15% zirconium and 85% titanium (Ti-15% Zr), and a high noble gold-palladium alloy

Clinical performance of titanium-zirconium implants with a hydrophilic surface in patients with controlled type 2 diabetes mellitus: 2-year results from a prospective case-control clinical study.

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Analyze the 2-year clinical performance of single-unit titanium-zirconium (TiZr) alloy narrow-diameter (3.3 mm) dental implants with a hydrophilic surface (Straumann® Roxolid®, SLActive®) in patients with controlled type 2 diabetes mellitus (T2DM), measured using the glycated

One-year follow-up of titanium/zirconium alloy X commercially pure titanium narrow-diameter implants placed in the molar region of the mandible: a randomized controlled trial.

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OBJECTIVE To analyze marginal bone loss (MBL) and clinical parameters around narrow-diameter implants (NDIs - 3.3 mm) made of titanium/zirconium alloy (TiZr) in comparison with commercially pure titanium (cpTi) installed in the molar region of the mandible after 1 year in function. METHODS Ten

Small-diameter titanium grade IV and titanium-zirconium implants in edentulous mandibles: five-year results from a double-blind, randomized controlled trial.

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BACKGROUND The aim of this study was to compare the 5-year survival and success rates of 3.3 mm dental implants either made from titanium-zirconium (TiZr) alloy or from Grade IV titanium (Ti Grade IV) in mandibular implant-based removable overdentures. METHODS The core study had a follow-up period

Small-diameter titanium Grade IV and titanium-zirconium implants in edentulous mandibles: three-year results from a double-blind, randomized controlled trial.

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OBJECTIVE The aim of this study was to compare crestal bone-level changes, soft tissue parameters and implant success and survival between small-diameter implants made of titanium/zirconium (TiZr) alloy or of Grade IV titanium (Ti) in edentulous mandibles restored with removable

Non-surgical treatment of peri-implant mucositis and peri-implantitis at two-piece zirconium implants: A clinical follow-up observation after up to 3 years.

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OBJECTIVE To assess the long-term clinical outcomes following non-surgical therapy of peri-implant diseases at two-piece zirconium implants. METHODS A total of 27 patients suffering from either (i) peri-implant mucositis (n = 24 implants), or (ii) peri-implantitis (n = 16 implants) completed a mean

[Clinical and roentgenologic outcome evaluation after apicoectomy with zirconium oxide ceramic pins--a prospective study of 112 apicoectomy teeth].

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We post-examined 112 apicectomies in 93 patients after an average placement period of 4.8 months (3-15.3 months) both clinically and radiologically in a prospective study to evaluate the security of success using zirconoxide ceramic pins. Clinical functioning was examined by means of the clinical

Non-surgical treatment of peri-implant mucositis and peri-implantitis at zirconia implants: a prospective case series.

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OBJECTIVE To assess the efficacy of non-surgical therapy for the management of peri-implant diseases at a two-piece zirconium implant system. METHODS Thirty-four patients with 45 implants participated in this study. Seventeen patients (24 implants) were diagnosed with peri-implant mucositis and

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