Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities

Hacettepe University

Status: Completed

Conditions: Tooth Diseases

Treatments: Device: Vertise Flow; Device: LuxaFlow; Device: Teco Adhesive

Study type: Interventional

Funder types: Other

Identifiers

NCT03556553

Vertise-Luxa Flow

Details and patient eligibility

About

The aim of this study is to evaluate long-term clinical performance of a self-adhering flowable resin composite in comparison with a conventional flowable resin composite used with an etch&rinse adhesive system in minimally invasive class I cavities. Twenty-five patients will receive at least one pair of class I restorations. After class I cavities were prepared they were restored either with a self-adhering flowable resin composite (VertiseFlow/Kerr-VR) or with a flowable resin composite (Luxaflow/DMG-LX) in combination with an etch&rinse adhesive (Teco/DMG) [according to the manufacturers' instructions. Restorations will be evaluated at baseline and yearly according to FDI criteria by two evaluaters. Statistical analysis will be carried out with Pearson Chi-Square test and Cochran Q-test followed by Mc Nemar's.

Enrollment: 25 patients

Sex: All

Ages: 16 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• having no medical or behavioral problems preventing then from attending review visits, absence of previously placed restorations,having antagonist teeth

Exclusion criteria

• poor gingival health,uncontrolled, rampant caries,bruxism,removable partial dentures, xerostomia

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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25 participants in 2 patient groups

Vertise Flow

Experimental group

Description:

Superficial Class I cavities restored with Vertise Flow

Treatment:

Device: Vertise Flow

LuxaFlow

Experimental group

Description:

Superficial Class I cavities restored with LuxaFlow

Treatment:

Device: Teco Adhesive

Device: LuxaFlow