Clinical Comparison of Different Flowable Resin Composites

NCT04324008 · tracked via the Priya Life Science Turkey tracker

Sponsor

Hacettepe University

Phase

Not applicable

Started

2017-11-01

Last updated

2025-12-03

Condition(s) studied

Tooth Diseases

Investigational drug(s) / intervention(s)

ConsticG-ænial Universal FloTetric N-Flow (self-etch)Tetric N-Flow (etch&rinse)

Constic: Flowable resin composite

G-ænial Universal Flo: Flowable resin composite

Tetric N-Flow (self-etch): Tetric N-Flow (Tetric N-Bond Universal, self-etch mode)

Tetric N-Flow (etch&rinse): Tetric N-Flow (Tetric N-Bond Universal, etch\&rinse mode)

Study summary

The aim of this study is to evaluate a self-adhesive flowable resin composite, a flowable resin composite with high viscosity and a conventional flowable resin composite in combination with a universal adhesive using two different application modes. All patients will receive at least 4 occlusal restorations. Cavities will be divided into four groups according to restorative systems used: Constic (a self-adhering flowable composite), G-ænial Universal Flo (a highly filled flowable composite), Tetric N-Flow (self-etch) (a conventional flowable composite), Tetrin N-Flow (etch\&rinse).

Eligibility

Sex

ALL

Min age

18 Years

Max age

65 Years

Healthy volunteers

Accepted

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

Primary outcome measure(s)

Clinical performances of different flowable resin composite — two years
Two year results according to USPHS criteria

Trial sites (1)

Facility	City	Region	Status
Hacettepe University	Ankara	Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04324008 on ClinicalTrials.gov ↗ ← All trials in Turkey