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

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT03556553

Enrollment

Registered

2018-06-14

Start date

2011-03-30

Completion date

2016-06-30

Last updated

2021-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth Diseases

Keywords

composite resin, occlusal caries

Brief summary

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.

Interventions

DEVICEVertise Flow

Composite resin

DEVICELuxaFlow

Composite resin

DEVICETeco Adhesive

Adhesive system

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

SINGLE (Subject)

Eligibility

Sex/Gender

ALL

Age

16 Years to 65 Years

Healthy volunteers

Yes

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

Design outcomes

Primary

Measure	Time frame	Description
Clinical performances of flowable composite resins	Five years	Five year results according to FDIcriteria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026