Fine-hybrid and nanohybrid restorative materials show similar durability in Class II cavities
- PMID: 20023616
- DOI: 10.1038/sj.ebd.6400683
Fine-hybrid and nanohybrid restorative materials show similar durability in Class II cavities
Abstract
Design: This was a randomised trial.
Intervention: Individuals who required a minimum of two replacement fillings were recruited. Restorations were placed using either Grandio bonded with Solobond M (Voco, Cuxhaven, Germany) or Tetric Ceram bonded with Syntac (Ivoclar Vivadent, Schaan, Liechtenstein).
Outcome measure: At the initial recall (baseline, ie, within 2 weeks), and after 6 months, 1 and 2 years, all restorations were assessed according to the modified United States Public Health Service (US PHS) criteria by two independent investigators using mirrors, probes, bitewing radiographs, impressions and intra-oral photographs. Recall assessments were not performed by the clinician who initially placed the restorations.
Results: Both recall rate and survival rate were 100% after 4 years of clinical service. No significant difference was found between the restorative materials. Hypersensitivities were significantly reduced over time (P < 0.05; Friedman test). A significant deterioration over time was found for the criteria of marginal integrity (66% sufficient after 4 years),tooth integrity (15% sufficient), filling integrity (73% sufficient) and proximal contact. Stereo light microscopy and scanning electron microscopy (SEM) analysis of restoration margins revealed differences in the amount of perfect margins in favour of Tetric Ceram (P <0.05).
Conclusions: Both materials performed satisfactorily over the 4-year observation period. Because of the extension of the restorations, wear was clearly visible after 4 years of clinical service with 50% sufficient ratings.
Comment on
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Nanohybrid vs. fine hybrid composite in Class II cavities: clinical results and margin analysis after four years.Dent Mater. 2009 Jun;25(6):750-9. doi: 10.1016/j.dental.2008.12.003. Epub 2009 Feb 23. Dent Mater. 2009. PMID: 19237189 Clinical Trial.
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