36-Month Clinical Evaluation of a Universal Adhesive

Status Completed

Clinical Trial 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.

Clinical Trial 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

Related Conditions & MeSH terms

Non-Carious Cervical Lesions

Clinical Trial Details

NCT number	NCT03932929
Study type	Interventional
Source	Hacettepe University
Contact
Status	Completed
Phase	N/A
Start date	September 2, 2015
Completion date	September 2, 2018

View Details

See also
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