Clinical Comparison of Different Adhesives in NCCLs

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

34 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-10

Study Completion Date

2026-06-10

Brief Summary

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The aim of this randomized, controlled, prospective clinical trial is to evaluate the performances of a universal adhesive in three different application modes, a self-etch adhesive and an etch\&rinse adhesive in restoration of non-caries cervical lesions. Thirty-four patients will receive restorations. Lesions will be divided into 5 groups according to adhesive systems and application modes: CU-SE: Clearfil Universal Bond Quick in self-etch mode, CU-SLE: Clearfil Universal Bond Quick in selective etch mode, CU-ER: Clearfil Universal Bond Quick in etch\&rinse mode, CSE: Clearfil SE Bond, TB: Tetric N-Bond. Restorations (Tetric N-Ceram composite) will be scored with regard to retention, marginal discoloration, marginal adaptation, recurrent caries and post operative sensitivity using modified USPHS criteria after 48 months. Two examiners who is not involved in the placement of restorations will conduct the evaluations. Descriptive statistics will be performed using Chi-square tests.

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Detailed Description

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Conditions

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Tooth Wear

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Adhesive systems

Intervention Type DEVICE

Clearfil Universal Bond Quick

Adhesive systems

Intervention Type DEVICE

Clearfil Universal Bond Quick

Adhesive systems

Intervention Type DEVICE

Clearfil SE Bond

Adhesive systems

Intervention Type DEVICE

Tetric N-Bond

Adhesive systems

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* being 18 years or older,
* having no medical or behavioral problems preventing then from attending review visits,
* having at least 5 tooth with NCCLs
* having antagonist teeth