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Clinical Trials/NCT06404398
NCT06404398CompletedNot Applicable

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

Tanta University1 site in 1 country20 target enrollmentStarted: July 19, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
20
Locations
1
Primary Endpoint
assess single and multi-shade direct composite resin veneers

Study Overview

Brief Summary

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

Detailed Description

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Masking Description

This clinical study was double-blind study as the evaluators who were not included in the restorative procedures and the patients were blinded to tested groups, but the operator wasn't blinded to these groups

Eligibility Criteria

Ages
18 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Good hygiene.
  • •Vital discolored anterior teeth

Exclusion Criteria

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

Arms & Interventions

OMNICHROMA

Experimental

one single shade

Intervention: OMNICHROMA, Ceram. x spectra (Other)

Ceram. x spectra

Experimental

multi- shade

Intervention: OMNICHROMA, Ceram. x spectra (Other)

Outcomes

Primary Outcomes

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

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohammed Abd El Ghany Mohammed

Assistant lecturer

Tanta University

Study Sites (1)

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