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Treatment Result of Zirconia Laminate Veneer

Surface Conditioning Effectiveness, Accuracy and Treatment Result of Zirconia Laminate Veneer

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06406582
Enrollment
50
Registered
2024-05-09
Start date
2023-09-25
Completion date
2025-12-31
Last updated
2025-02-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cracked Tooth Syndrome, Dislocation, Tooth, Teeth, Endodontically-Treated, Tooth Abnormalities, Tooth Crowding, Tooth Fracture, Tooth Injuries

Keywords

ceramic laminate veneers, zirconia, lithium disilicate, computer-aided manufacturing

Brief summary

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

Detailed 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 double-blind manner (participants and the outcomes assessor) 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.

Interventions

DEVICEZirconia laminate veneer

Zirconia veneers are milled with computer-aided manufacturing technology from multilayered zirconia discs with shade matched with adjacent teeth. After sintering, veneer surfaces are treated with a hydrofluoric acid-nitric acid mixture. Next, veneers are cut back if necessary to provide space for characterization. Veneers are bonded with a light-cured veneer adhesive system (Relyx Veneer LC, 3M, USA).

DEVICELithium Disilicate laminate veneer

Lithium Disilicate veneers are milled with computer-aided manufacturing technology from lithium disilicate blocks with shade matched with adjacent teeth. After sintering, veneer surfaces are treated with hydrofluoric acid. Next, veneers are cut back if necessary to provide space for characterization. Veneers are bonded with a light-cured veneer adhesive system (Relyx Veneer LC, 3M, USA).

Sponsors

Hanoi Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Double-blind. Both participants and the outcomes assessor are kept unaware of which ceramic laminate veneer material (Zirconia or Lithium Disilicate) the participants are receiving

Intervention model description

Zirconia Group (Intervention): Participants receive zirconia laminate veneers. Lithium Disilicate Group (Control): Participants receive lithium disilicate laminate veneers. Lithium disilicate is a standard ceramic material for laminate veneers.

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Spaced tooth * Discolored tooth * Malformed tooth * Root canal-treated tooth * Chipped tooth * Mildly crowded tooth

Exclusion criteria

* Tooth bruxism * Inadequate enamel for bonding * Large restoration exists * Bad oral habits harming restoration

Design outcomes

Primary

MeasureTime frameDescription
Evaluation criteria based on the modified United States Public Health Standard2 weeks, 6 months, 12 monthsShade match, contour, fracture, loss of retention, hypersensitivity
Marginal and internal fitBefore veneer adhesionMeasurement of marginal and internal fit in micrometers with silicone replica method
Gingival health2 weeks, 6 months, 12 monthsAssessment of gingival index
Periodontal pocket2 weeks, 6 months, 12 monthsMeasurement of periodontal pocket depth in millimeters

Countries

Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026