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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).
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
Yes
Hacettepe University
Ankara, Turkey (Türkiye)
Start Date
November 1, 2017
Primary Completion Date
January 1, 2018
Completion Date
November 1, 2026
Last Updated
December 3, 2025
28
ACTUAL participants
Constic
DEVICE
G-ænial Universal Flo
DEVICE
Tetric N-Flow (self-etch)
DEVICE
Tetric N-Flow (etch&rinse)
DEVICE
Lead Sponsor
Hacettepe University
NCT05220865
NCT06895915
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05792800