
The high demands on the clinical performance of a single-tooth provisional restoration necessitate that said performance be examined. The authors evaluated 24 teeth evaluated. Two test groups received bis-acrylic composite for provisional crowns (n = 12) and a single-unit, self-supporting, malleable, light-curing composite crown (n = 12). Final crowns (n = 24) served as paired controls. Evaluation of clinical success was measured using previously selected subcategories of FDI criteria. Statistical analysis was performed using McNemar's Test (α = 0.05). The null hypothesis of no improvement of the definitive crown relative to the provisionals was rejected at the 5% significance level (McNemar's P value <.001, Bonferroni corrected). Of the provisional crowns, 75% received a clinically insufficient valuation, while only 8% of the definitive crowns did. The authors concluded that, independent of the manufacturing process, a bis-acrylic composite provisional crown cannot serve as a replacement for a conventionally manufactured definitive crown.
Adult, Aged, 80 and over, Male, Adolescent, Crowns, Acrylic Resins, Middle Aged, Composite Resins, Dental Restoration, Temporary, Young Adult, Treatment Outcome, Materials Testing, Humans, Female, Aged
Adult, Aged, 80 and over, Male, Adolescent, Crowns, Acrylic Resins, Middle Aged, Composite Resins, Dental Restoration, Temporary, Young Adult, Treatment Outcome, Materials Testing, Humans, Female, Aged
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