Clinical Performance of Restorative Materials in Primary Teeth

Status Not yet recruiting

Clinical Trial Summary

The purpose of this study is to evaluate and compare the clinical performance of dental restorative materials in Class II cavities of primary molar teeth

Clinical Trial Description

Restorations will be placed on four primary molar teeth with proximal caries, in a split mouth design. 100 patients will be included in the study. The teeth will be randomized into four groups according to the restorative materials. Group 1: Adhesive agent+ Compomer (Dyract AP, Dentsply DeTrey, Konstanz,Germany) Group 2: Primer + Resin modified glass ionomer (Vitremer, 3M ESPE, U.S.) Group 3: Adhesive agent + Giomer (Beautifil II, (Shofu Dental, Tokyo, Japan) Group 4: Amalgam (Permite amalgam, SDI Limited, Bayswater, Australia) The restorations will be evaluated at baseline, 3., 6., 12. months for the first year, and at every 6 months for 5 years. The modified US Public Health Service criteria (secondary caries, marginal integrity, marginal discoloration and retention) will be used for clinical evaluation of restorations. The data will be analysed statistically using Wilcoxon test, chi square test and the Kaplan-Meier survival method will be used to estimate survival percentages. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03037814
Study type	Interventional
Source	Hacettepe University
Contact	Zafer C Cehreli, DDS, PhD
Phone	00905353197969
Email	zcehreli@gmail.com
Status	Not yet recruiting
Phase	N/A
Start date	September 28, 2021
Completion date	March 25, 2027

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