Efficiency of Different Modes of Universal Adhesive

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to evaluate and compare the clinical performance of a Universal adhesive's different application modes.

Clinical Trial Description

Class 2 composite restorations will be placed using a bulk-fill composite resin restorative on two posterior teeth with proximal caries, in a split mouth design. 25 patients will be included in the study. The teeth will be randomized into two groups according to the application mode of universal adhesive material.

Group 1: the universal adhesive will be used in etch-and-rinse mode Group 2: the universal adhesive will be used in self-etch mode. The US Public Health Service criteria (secondary caries, anatomical form, surface roughness, marginal integrity, marginal discoloration and retention) will be used for clinical evaluation of atraumatic resin restorations. The restorations will be evaluated at baseline and 6th, 12th, 18th, 24th months. Intra-oral photos will be taken directly after treatment and at control appointments to evaluate discoloration and seconder caries under magnification.

The data will be analysed statistically using Fisher's Exact Test; and the Kaplan-Meier and Wilcoxon method will be used to estimate survival percentages. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04271150
Study type	Interventional
Source	Hacettepe University
Contact
Status	Active, not recruiting
Phase	N/A
Start date	May 1, 2018
Completion date	May 1, 2025

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