36-Month Clinical Evaluation of a Universal Adhesive

2019-05-05 16:45:30 | BioPortfolio


The aim of this clinical trial was to evaluate and compare the performance of a universal adhesive with different adhesive strategies in the restoration of non-carious cervical lesions (NCCLs) over a 36-month period.


One hundred sixty-five NCCLs in 35 patients (13 female, 22 male) with at least 3 lesions were included in this study. Three groups were formed according to adhesive strategies used (n=55): selective-etch mode; etch-and-rinse mode (ER); or self-etch (SE) mode of a universal adhesive, Single Bond Universal. The same nanofilled resin composite, Filtek Ultimate was used for all restorations by a single operator. The restorations were evaluated by two calibrated examiners at baseline and at 6-, 12-, 18-, 24- and 36- months in accordance with the modified USPHS criteria. The Chi-square test was used for intergroup, the Cochran Q test was used for intragroup comparison.

Study Design


Application Strategies of a Universal Adhesive on Non-carious Cervical Lesions


Scotchbond Universal Adhesive (3M ESPE, St. Paul, MN, USA)


Hacettepe University




Hacettepe University

Results (where available)

View Results


Published on BioPortfolio: 2019-05-05T16:45:30-0400

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