BACKGROUND: The aim of this randomized controlled study was to evaluate the clinical performance of a highly filled flowable composite compared to a conventional paste-type composite in direct posterior restorations after 36 months. METHODS: A total of 58 mid-size to extensive posterior composite restorations were randomly placed in 32 patients, mean age of 43.9 years (range 25-76), using either a conventional composite Estelite Sigma Quick (Conventional) or a highly filled flowable composite G-aenial Universal Flo with a two-step self-etch adhesive. The restorations were evaluated after placement (baseline) and at 6, 12, 24 and 36 months according to the FDI criteria. RESULTS: At the 36-month follow-up, 42 restorations were evaluated in 21...
Colak, Hakan/0000-0001-8262-0913; Bayraktar, Yusuf/0000-0001-6250-5651; Hamidi, Mehmet Mustafa/0000-...
The wear of five posterior composites at occlusal contact areas (OCA) and contact free occlusal area...
Objective: The aim of this investigation was to evaluate the clinical performance of a new compomer ...
Objective: The aim of this study was to evaluate the 2-year clinical performance of class II restora...
Background. Research has suggested that packable resin-based composites inserted with a placement te...
Background The authors evaluated clinical performances of a packable and a conventional hybrid resi...
Objective The purpose of this prospective randomized clinical study was to compare the clinical perf...
This study evaluated the 3-year clinical performance of four different flowable composite materials ...
WOS: 000488851900004PubMed ID: 31579892Purpose The aim of this study was to evaluate and compare the...
Objectives: The aim of this study was to evaluate the clinical performance of a nanohybrid and a mic...
OBJECTIVES: This retrospective longitudinal study investigated the longevity of posterior restoratio...
WOS: 000183934100003PubMed ID: 12859086Objectives: The aim of this study was to investigate the clin...
This clinical study evaluated the retention and caries protection of a flowable resin composite (Flo...
Bulk-fill restorative materials such as bulk-fill composite resins and high viscous glass ionomer ce...
OBJECTIVES: This randomized controlled clinical trial evaluated the 3-year clinical performance of a...
Colak, Hakan/0000-0001-8262-0913; Bayraktar, Yusuf/0000-0001-6250-5651; Hamidi, Mehmet Mustafa/0000-...
The wear of five posterior composites at occlusal contact areas (OCA) and contact free occlusal area...
Objective: The aim of this investigation was to evaluate the clinical performance of a new compomer ...
Objective: The aim of this study was to evaluate the 2-year clinical performance of class II restora...
Background. Research has suggested that packable resin-based composites inserted with a placement te...
Background The authors evaluated clinical performances of a packable and a conventional hybrid resi...
Objective The purpose of this prospective randomized clinical study was to compare the clinical perf...
This study evaluated the 3-year clinical performance of four different flowable composite materials ...
WOS: 000488851900004PubMed ID: 31579892Purpose The aim of this study was to evaluate and compare the...
Objectives: The aim of this study was to evaluate the clinical performance of a nanohybrid and a mic...
OBJECTIVES: This retrospective longitudinal study investigated the longevity of posterior restoratio...
WOS: 000183934100003PubMed ID: 12859086Objectives: The aim of this study was to investigate the clin...
This clinical study evaluated the retention and caries protection of a flowable resin composite (Flo...
Bulk-fill restorative materials such as bulk-fill composite resins and high viscous glass ionomer ce...
OBJECTIVES: This randomized controlled clinical trial evaluated the 3-year clinical performance of a...
Colak, Hakan/0000-0001-8262-0913; Bayraktar, Yusuf/0000-0001-6250-5651; Hamidi, Mehmet Mustafa/0000-...
The wear of five posterior composites at occlusal contact areas (OCA) and contact free occlusal area...
Objective: The aim of this investigation was to evaluate the clinical performance of a new compomer ...