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Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities

Tooth Diseases Clinical Trial

Official title:
Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities

Clinical Trial Summary

The aim of this study is to evaluate long-term clinical performance of a self-adhering flowable resin composite in comparison with a conventional flowable resin composite used with an etch&rinse adhesive system in minimally invasive class I cavities. Twenty-five patients will receive at least one pair of class I restorations. After class I cavities were prepared they were restored either with a self-adhering flowable resin composite (VertiseFlow/Kerr-VR) or with a flowable resin composite (Luxaflow/DMG-LX) in combination with an etch&rinse adhesive (Teco/DMG) [according to the manufacturers' instructions. Restorations will be evaluated at baseline and yearly according to FDI criteria by two evaluaters. Statistical analysis will be carried out with Pearson Chi-Square test and Cochran Q-test followed by Mc Nemar's.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03556553
Study type Interventional
Source Hacettepe University
Contact
Status Completed
Phase N/A
Start date March 30, 2011
Completion date June 30, 2016
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