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Clinical Trial Summary

The clinical performance of an an alkasite-based restorative material and two different resin composites will be evaluated and compared in non-carious cervical lesions. After recruiting participants with at least three non-carious cervical lesions, all restorations will be placed by a single clinician. Lesions will be divided in three groups: an alkasite-based restorative material (Cention N, Ivoclar Vivadent, Schaan, Liechtenstein (CN)), hybrid resin composite (Gradia Direct Anterior, GC, Tokyo, Japan (GD)) and a highly filled flowable resin composite ((G-aenial Universal Flo, GC, Tokyo, Japan (GF)). All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria. Descriptive statistics will be performed using chi-square tests.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06375837
Study type Interventional
Source Hacettepe University
Contact Fatma Oz
Phone 903123052270
Email dilsadoz@hacettepe.edu.tr
Status Recruiting
Phase N/A
Start date April 15, 2024
Completion date June 15, 2026

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