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Clinical Evaluation of Color Stability of Direct Composite Resin Veneers in Vital Anterior Teeth

Clinical Evaluation of Color Stability of Direct Composite Resin Veneers in Vital Anterior Teeth

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06510400
Enrollment
20
Registered
2024-07-19
Start date
2022-07-19
Completion date
2024-04-09
Last updated
2024-07-24

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

Conditions

Tooth Discoloration

Brief summary

Assess color stability of direct veneers over an 18-month recall periods

Detailed description

In today's restorative dentistry, aesthetics has become essential. The primary determinants of the aesthetics of natural teeth are color and form. The significance of color in dental science has greatly increased during the past few decades. Techniques to restore teeth to their natural appearance have been developed in direct response to patient demand for cosmetic dental procedures. In contemporary cosmetic dentistry, discolorations are often seen as an aesthetic concern. In order to correct cosmetic flaws in color and form, direct laminate veneers entail the creative application of resin composite material to the tooth surfaces. Because they may be completed chairside, are readily repaired, and have abrasion rates that are similar to those of real teeth, they are viewed as competitors to ceramic veneers. With direct resin composite veneers, color stability is thought to be a common clinical issue that reduces the aesthetic result over an extended period of clinical service. The capacity of any dental material to retain its original color is known as color stability. The clinical restoration process is streamlined with the introduction of universal composites, which also considerably reduce chair-side time and simplify the color matching such as OMNICHROMA.

Interventions

supra nano filled composite

nano hybrid composite resin

Sponsors

Tanta University
Lead SponsorOTHER

Study design

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

Masking description

double blinded

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* have good hygiene. * No medical diseases * discolored vital anterior teeth

Exclusion criteria

* para functional activities. * non vital teeth. * severe intrinsic discoloration.

Design outcomes

Primary

MeasureTime frameDescription
Color stability evaluation18 monthsTwo calibrated evaluators who were not engaged in the insertion of veneer restorations used VITA Easyshade V to measure the color (ΔE). The device was calibrated before reading.

Countries

Egypt

Outcome results

None listed

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