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Assessment of Anterior Teeth Restored With Ultra-translucent Multilayer Zirconia vs Lithium Disilicate Laminate Veneers

Clinical Assessment of Anterior Teeth Restored With Ultra-translucent Multilayer Zirconia Versus Lithium Disilicate Laminate Veneers (Randomized Clinical Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04598737
Enrollment
26
Registered
2020-10-22
Start date
2020-10-18
Completion date
2021-11-30
Last updated
2020-10-22

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

Conditions

Retention, Color Match, Marginal Adaptation and Restoration Integrity

Brief summary

The aim of the present study is to assess the clinical performance of multilayered translucent zirconia laminate veneers versus lithium disilicate laminate veneers in terms of modified USPHS criteria for assessment of dental restorations (retention, restoration integrity, color match and marginal adaptation)

Detailed description

inferior mechanical properties of glass ceramics necessities the continuous development and modification for materials suitable for all clinical situations multilayered translucent zirconia provides the advantages of high mechanical properties than all glass ceramic in addition to the improved translucency in the new generations. Therefore, the purpose of the present study is to evaluate the clinical performance of newly introduced multilayered translucent zirconia as a monolithic laminate veneer in comparison with lithium disilicate laminate veneer to determine the clinical functional and structural integrity of the restoration

Interventions

PROCEDUREUltra-translucent multilayer zirconia

Ultra-translucent multilayer zirconia laminate veneer treatment

Lithium disilicate laminate veneer treatment

Sponsors

Cairo University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* sufficient sound enamel thickness * Presence of one adjacent natural teeth that doesn't need laminate to compare shade * age range 20 to 40 years old * non smokers * diastema less than 2mm * tooth fracture not exceeding incisal one third * normal occlusion * vital teeth * healthy periodontal tissues

Exclusion criteria

* -insufficient enamel thickness * restoration more than 40 % of tooth surface * parafunctional habits * deep discoloration * sever teeth rotation * edge to edge or deep bite * abnormal occlusion * bad oral hygiene

Design outcomes

Primary

MeasureTime frameDescription
Retention12 months follow up periodassessment of restoration will be done for retention on the base of of modified USPHS criteria for assessment of dental restorations

Secondary

MeasureTime frameDescription
Restoration integrity12 months follow up periodassessment of restoration will be done for restoration integrity on the base of of modified USPHS criteria for assessment of dental restorations

Other

MeasureTime frameDescription
Color match12 months follow up periodassessment of restoration will be done for color match on the base of of modified USPHS criteria for assessment of dental restorations
Marginal adaptation12 months follow up periodassessment of restoration will be done for Marginal adaptation on the base of of modified USPHS criteria for assessment of dental restorations

Outcome results

None listed

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