Aim: To report the 10-year clinical and radiographic outcomes of implants placed in grafted (GBR) and non-grafted (no-GBR) sites in a Swiss specialist private practice using hydrophilic implants with a low surface roughness flange.
Methods: Fifty consecutively enrolled patients received 159 hydrophilic implants with a low surface roughness flange. A first re-evaluation was performed 1 year after delivery of restoration (T1).
Background: Ongoing marginal bone loss is a threat to the longevity of implant-supported prostheses.
Aim: The aim of the present study was to retrospectively evaluate the survival rate and factors affecting marginal bone levels at a hydrophilic implant design after 5 years in function.
Materials And Methods: The study group consisted of 51 consecutive patients previously treated with 159 hydrophilic implants (Neoss Straight Proactive implants) and scheduled for annual check-ups with clinical and radiographic examinations during 5 years.
Clin Implant Dent Relat Res
June 2016
Purpose: The aim of the present 1-year clinical and radiographic study was to evaluate a hydrophilic dental implant when used in everyday cases in one clinic. The purpose was also to compare augmented with nonaugmented sites.
Materials And Methods: The study group consisted of 50 consecutive patients treated with 159 dental implants (Proactive, Neoss Ltd, Harrogate, UK) in both mandibles and maxillae.
Clin Implant Dent Relat Res
August 2012
Background: New dental implant systems are continuously introduced to the market. It is important that clinicians report their experiences with these implants when used in different situations.
Aim: The study aims to report the outcomes from a retrospective study on Neoss implants when used with or without guided bone regeneration (GBR) procedures.