Bruxism Clinical Trial
Official title:
24-Month Performance of a Glass-hybrid-restorative in Non-carious Cervical Lesions of Patients With Bruxism: A Split-mouth, Randomized Clinical Trial
This is a double blinded, split mouth, randomized clinical study that evaluated the performance of a glass hybrid restorative material in non-carious servical lesions in patients with bruxism. The lesions were restored with glass hybrid restorative (Equia Forte) or nano ceramic composite resin (Ceram-x One). Restorations were evaluated after 24 months according to USPHS criteria and the data were evaluated.
The aim of this study was to evaluate the clinical performance of a glass-hybrid-restorative
compared with a nano ceramic composite resin in non-carious cervical lesions (NCCLs) of
patients with bruxism.
For this purpose, twenty-five patients having NCCLs and bruxism enrolled to the present
study. Before treatment, the dimensions of the NCCLs were measured in depth, gingival-incisal
height and mesio-distal width using a CPI probe. Degree of tooth wear (TWI) and gingival
conditions (GI) are also recorded. A total of 148 NCCLs were randomly restored with a a
glass-hybrid-restorative system (Equia Forte Fil, GC, Tokyo, Japan) or a nano ceramic
composite resin (Ceram.X One Universal, Dentsply, DeTrey, Konstanz, Germany) and restorations
were evaluated at baseline and after 6,12 and 24 months according to the modified-USPHS
criteria. Data were analyzed with Chi- Square, Fisher's Exact Test, Mann Whitney-U and
Cochran's Q tests (p < 0.05).
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