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36-Month Clinical Evaluation of a Universal Adhesive

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

Summary

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.

Description

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

Conditions

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

Intervention

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

Location

Hacettepe University
Ankara
Turkey
06100

Status

Completed

Source

Hacettepe University

Results (where available)

View Results

Links

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

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