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

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.

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Key information

Conditions

Tooth Diseases Stomatognathic Diseases

Age range

16 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Vertise Flow

Device

Composite resin

Other names: Self-adhering flowable composite

LuxaFlow

Device

Composite resin

Other names: Flowable composite with Teco adhesive system

Teco Adhesive

Device

Adhesive system

Primary outcomes

Clinical performances of flowable composite resins

Time frame: Five years

Five year results according to FDIcriteria

Sponsors and collaborators

Lead sponsor

Hacettepe University

Other

Registry information

Important dates

Study start: 2011
Primary completion: 2011
Study completion: 2016
First posted: Jun 14, 2018
Registry last updated: Sep 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed