NCT03932929

36-Month Clinical Evaluation of a Universal Adhesive

36-Month Clinical Evaluation of Different Adhesive Strategies of a Universal Adhesive

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 35 (actual)
• Sponsor: Hacettepe University · Academic / Other
• Sex: All
• Age: 18 Years – 81 Years
• Healthy volunteers: Accepted

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.

Detailed 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.

Conditions

• Non-Carious Cervical Lesions

Interventions

Type	Name	Description
DEVICE	Scotchbond Universal Adhesive (3M ESPE)	Adhesive system

Timeline

• Start date: 2015-09-02
• Primary completion: 2018-09-02
• Completion: 2018-09-02
• First posted: 2019-05-01
• Last updated: 2019-05-06

Locations

1 site across 1 country: Turkey (Türkiye)