Evaluation of the Initial Color Match of Different Single-shade Composites

NCT ID: NCT06473727

Last Updated: 2024-06-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-05-24

Study Completion Date

2024-06-16

Brief Summary

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The aim of this study was to evaluate the initial colour match of anterior non-carious cervical lesions restored with different single-shade resin composites, namely Omnichroma (Tokuyama) and Charisma Topaz One (Kulzer).

Detailed Description

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Colour selection for composite restorations is a challenging process influenced by a number of environmental and operator factors. The polychromatic structure of natural teeth presents a challenge to shade selection. Consequently, the prevailing trend towards simplification of shade matching has led to the emergence of single-shade universal composites. Single-shade universal composites are able to replicate the natural colour of teeth by capturing the structural colour based on the size of the filler particles. Unlike other materials, it does not require the use of additional dyes or pigments. The blending, colour induction and colour assimilation effects of resin composites are collectively referred to as the chameleon effect. This phenomenon allows resin-based restorative materials to achieve a shade that closely resembles the colour of the surrounding tooth structure. The intelligent monochromatic composite makes shade selection easier for the clinician and provides a quick and easy way to create aesthetic restorations. Its distinctive character reduces confusion and potentially saves time in the clinic. However, the effectiveness of this material in matching different shades of natural teeth remains uncertain, and there is a paucity of clinical evidence on the efficacy of its colour-matching capabilities in dental restorations.

Conditions

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Dental Diseases

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Two groups
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Omnichoroma

Anterior non-carious cervical lesions restored with Omnichoroma single-shade resin composite.

Group Type ACTIVE_COMPARATOR

Omnichoroma

Intervention Type OTHER

Patients with anterior non-carious cervical lesions were treated with Omnichoroma. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.

Charisma Topaz One

Anterior non-carious cervical lesions restored with Charisma Topaz One single-shade resin composite.

Group Type ACTIVE_COMPARATOR

Charisma Topaz One

Intervention Type OTHER

Patients with anterior non-carious cervical lesions were treated with Charisma Topaz One. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.

Interventions

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Omnichoroma

Patients with anterior non-carious cervical lesions were treated with Omnichoroma. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.

Intervention Type OTHER

Charisma Topaz One

Patients with anterior non-carious cervical lesions were treated with Charisma Topaz One. Colour measurements were taken from the middle third of the teeth to be treated using a spectrophotometer. The initial colour measurement was taken from the middle third of the restoration made in the same place and at the same time 24 hours after treatment.

Intervention Type OTHER

Other Intervention Names

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Group 1 Group 2

Eligibility Criteria

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Inclusion Criteria

* Maintain satisfactory oral hygiene
* Have healthy gingival tissues
* Presence of an anterior non-carious cervical lesion approximately 5 m wide

Exclusion Criteria

* Presence of caries
* Signs of fistula
* Pulp exposure
* Periodontal tissue swelling
* Abnormal tooth mobility
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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TC Erciyes University

OTHER

Sponsor Role lead

Responsible Party

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Ayse Nur Dogan

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ayse Nur Dogan

Role: PRINCIPAL_INVESTIGATOR

TC Erciyes University

Locations

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Faculty of Dentistry, Erciyes University

Kayseri, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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ErciyesU-DF-AD-01

Identifier Type: -

Identifier Source: org_study_id

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