Clinical Evaluation of Four Aesthetic Restorations in Non-carious Cervical Lesions

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

WITHDRAWN

Clinical Phase

NA

Study Classification

INTERVENTIONAL

Study Start Date

2019-07-31

Study Completion Date

2021-05-31

Brief Summary

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To compare the clinical performance of high-viscosity glass ionomer, flowable composite, bulkfill composite and nanohybrid composite restorations in non-carious cervical lesions (NCCLs).

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Detailed Description

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One hundred fourty NCCLs were randomised into four groups according to a split-mouth design. Clinical evaluations will be performed after 1 week, 3 months, 6 months, using FDI (World Dental Federation) criteria.

Conditions

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Noncarious Cervical Lesions

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Apply cavity conditioner (20% polyacrylic acid) 10 s on enamel and dentine, rinse Mix 10 s and apply bulk-fill Apply EQUIA coat and light cure for 20 s

unit

Intervention Type OTHER

Clearfil Majesty Esthetic

Apply in 2-mm increment, light cure for 20 s

Intervention Type OTHER

NexComp Flow

Apply in 2-mm increment light cure for 20 s

Intervention Type OTHER

3M Espe Bulk-fill

Apply in single increment up to 4 mm; light curing for 20 s

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* had at least four non-carious symmetrical cervical lesions,
* had permanent dentition and were older than 20 years old,
* had cervical margins in dentin