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Clinical Trial Summary

This study aims to evaluate the clinical performance of the zirconia laminate veneer, a minimally invasive prosthetic restoration


Clinical Trial Description

Patients with indications for single tooth restoration with ceramic laminate veneers are recruited for the study. These indications include spaced, discolored, malformed, root canal-treated, chipped, and mildly crowded teeth. After providing written informed consent, all patients are randomly divided into two groups in a single-blind manner (participant) in a 1:1 ratio, including the Zirconia group (intervention) and the Lithium Disilicate group (control). Each patient's tooth is prepared and restored with the corresponding laminate veneer material, that is, zirconia and lithium disilicate. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06406582
Study type Interventional
Source Hanoi Medical University
Contact
Status Recruiting
Phase N/A
Start date September 25, 2023
Completion date December 31, 2025

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