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Clinical Trial Summary

The aim of this study is to evaluate the clinical performance of a nano-fill and a bulk fill resin composite in class II restorations.


Clinical Trial Description

In accordance with a split-mouth design, 50 patients will be received at least one pair of restorations, restored with a nanofill resin composite (Filtek Ultimate [FU]) and with a bulk fill resin composite (Tetric EvoCeram Bulk Fill [TB]). Each restorative resin will be used with its respective adhesive system according to the manufacturers' instructions. A total of 104 class II restorations will be placed by two operators. The restorations will be blindly evaluated by two examiners at baseline and at 1-, 2-, 3-, 4-, 5-, 6-, 7- and 8- year using modified US Public Health Service Ryge criteria. The comparison of the two restorative materials for each category will be performed with the chi-square test (a=0.05). The baseline scores will be compared with those at the recall visits using the Cochran Q-test. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04320576
Study type Interventional
Source Hacettepe University
Contact
Status Active, not recruiting
Phase N/A
Start date May 1, 2013
Completion date May 1, 2025

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