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Clinical Trial Summary

The aim of this study is to evaluate a self-adhesive flowable resin composite, a flowable resin composite with high viscosity and a conventional flowable resin composite in combination with a universal adhesive using two different application modes. All patients will receive at least 4 occlusal restorations. Cavities will be divided into four groups according to restorative systems used: Constic (a self-adhering flowable composite), G-ænial Universal Flo (a highly filled flowable composite), Tetric N-Flow (self-etch) (a conventional flowable composite), Tetrin N-Flow (etch&rinse).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04324008
Study type Interventional
Source Hacettepe University
Contact
Status Active, not recruiting
Phase N/A
Start date November 1, 2017
Completion date November 1, 2024

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