Trial reportClinical oral investigations2021
Randomized controlled clinical trial of a highly filled flowable composite in non-carious cervical lesions: 3-year results.
Trial report in Clinical oral investigations, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07128589 (Clinical Evaluation of 3M), which is not on this map. Cited by 6 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Clinical Evaluation of 3M(TM) Filtek(TM) Supreme Flowable Composites for Class IV and Veneers
Who cites it
6 citing papers in PubMed.
- Eight-year clinical evaluation of two types of resin composite in non-carious cervical lesions.Clinical oral investigations · 2022Trial
- One-Year Clinical Performance of Injectable and Paste-Type Composite Resins in Non-Carious Cervical Lesions Prepared with Er,Cr:YSGG Laser and Acid Etching: A Randomized Clinical Trial.Journal of functional biomaterials · 2026Article
- Highly Filled Flowable Composite Resins as Sole Restorative Materials: A Systematic Review.Materials (Basel, Switzerland) · 2025Review
- The impact of using two fiber-reinforced composites with different placement methods on the flexural strength of two resin materials: an in vitro study.BMC oral health · 2025Article
- Marginal Adaptation of Flowable vs Sonically Activated or Preheated Resin Composites in Cervical Lesions.The journal of adhesive dentistry · 2022Article
- Patients´ satisfaction concerning direct anterior dental restoration.Brazilian dental journalArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
objectivesThis prospective, randomized, split-mouth clinical trial assessed the 3-year clinical performance of a highly filled flowable composite and a conventional paste-type composite in non-carious cervical lesions (NCCLs). MATERIALS AND
methodsA total of 84 NCCLs in 27 subjects were included in this split-mouth design study and randomly divided into two groups: a highly filled flowable composite Clearfil Majesty ES Flow group (ES, n = 42) and a conventional paste-type composite Majesty group (MJ, n = 42). Clearfil SE Bond was used following the manufacturer's instructions. The restorations were evaluated at baseline (BL) and 1, 2, and 3 years using FDI (World Dental Federation) criteria. Data were analysed by a paired chi-squared test for intergroup comparisons and the Friedman test for intragroup comparisons (α = 0.05).
resultsBoth groups had a 97.3% retention rate at the 3-year evaluation. The acceptable scores (FDI scores 1-3) for each criterion exhibited no significant difference between the MJ and ES groups at any time point (p = 1.00). The marginal adaptation performance of ES was significantly better than that of MJ at every evaluation point (p < 0.05).
conclusionsThe 3-year clinical performance of ES in NCCLs was similar to that of MJ. When the restorations were clinically acceptable, ES showed better marginal adaptation than MJ. CLINICAL RELEVANCE: Compared with conventional paste-type composites, highly filled flowable composites showed similar clinical performance and better marginal adaptation for restoring NCCLs after 3 years.
trial registrationTRN: ChiCTR1900028484 . Date of registration: December 22, 2019, retrospectively registered.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.