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OpenTrials
Completed

NCT Number: NCT06404398

Clinical Evaluation of Single Versus Multi-Shade Direct Composite Resin Veneers

The aim of this study was to clinically evaluate single and multi-shade direct veneers.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Restorative Department, Faculty of Dentistry, Tanta University

Tanta, 31527, Egypt

About this study

The use of direct, light-activated resin composites in esthetic restorative dentistry has grown dramatically in response to growing needs. Recent developments have resulted in the creation of restorative materials and methods that, particularly in the anterior area, attempt to restore the natural appearance of the teeth.

Numerous clinical conditions, including tooth discolorations, severe fractures, misaligned teeth, and dental caries lesions, can significantly affect smile harmony and esthetic appearance, which can lower quality of life.

Modern cosmetic dentistry began with the introduction of laminate veneers in the 1970s, which combined the ideas of tooth conservation and aesthetics. Because laminate veneers (LVs) offer the potential to satisfy the need for extremely beautiful, minimally invasive, long-lasting restorations with superior clinical performance, they have gained popularity as a treatment option.

Direct composite veneering preserves natural tooth structure, may be completed chairside, doesn't require repeated appointments, doesn't require luting agents, is minimally invasive, readily repaired, and is less expensive because there are no laboratory fees. Furthermore, their abrasion rates are comparable to those of real tooth structures.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Good hygiene.
  • Vital discolored anterior teeth

Exclusion criteria

  • severe discoloration
  • Para functional activities
  • Non-vital teeth.
  • Pregnancy

Treatment and study plan

OMNICHROMA, Ceram. x spectra

Other

Each patient had two types of veneers.

Primary outcomes

  1. assess single and multi-shade direct composite resin veneers

    Time frame: 18 months evaluation periods

    Two evaluators assessed the restorations based on modified United States Public Health Service criteria. Score(0) represents ideal clinical scenario, Score(1) acceptable, Score (2) satisfactory, and Score(3) and Score (4) considered clinically unsatisfactory

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
May 8, 2024
Registry last updated
Jul 24, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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