Clarissa Calil Bonifácio

Dr. Clarissa Calil Bonifácio

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Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 August 2009 in Australian Dental Journal
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CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
CKCj Kleverlaan
Cj Kleverlaan
DRDaniela Raggio
Daniela Raggio
AWA Werner
A Werner
RCRcr De Carvalho
Rcr De Carvalho
WAWe Van Amerongen
We Van Amerongen

28 May 2014 in BMC Oral Health
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Journal Article
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Daniela HesseDaniela Hesse
Daniela Hesse
CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
FMFausto Mendes
Fausto Mendes
MBMariana Minatel Braga
Mariana Minatel Braga
JIJosé Carlos Pettorossi Imparato
José Carlos Pettorossi Imparato
DRDaniela Raggio
Daniela Raggio
The resin-based pit and fissure sealant is considered a successful tool in caries prevention, however there is a growing evidence of its use in controlling already established caries in posterior teeth. The aim of this clinical trial is to verify the efficacy of pit and fissure sealants in arresting dentinal caries lesions compared to partial excavation and restorative treatment in primary molar teeth.

30 November 2011 in Acta Odontologica Scandinavica
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CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
AWArie Werner
Arie Werner
CKCornelis Johanes Kleverlaan
Cornelis Johanes Kleverlaan
Objectives. The objective of this study was to investigate the effect of a nanofilled resin coat on the flexural strength (FS) and the early wear (after 50 000 and 200 000 cycles) of the glass-ionomer cements Fuji IX GP Extra (FIXE) and Ketac Molar Aplicap (KM). Materials and methods. Specimens were prepared and half of them were coated with G-Coat plus. The uncoated specimens were used as controls. Flexural strength (n = 10) was evaluated after 24 h using a 3-point bending test on a universal testing machine (ISO 9917-2). Wear (n = 20) was evaluated after 50 000 and 200 000 cycles using the ACTA wear machine. One-way, two-way ANOVA and Tukey post-hoc tests were used to analyze differences in FS and wear. Results. For FIXE the coat significantly increased the FS and the wear along the two time spans. KM did not show a significant difference in FS with the coat. Improvements in wear were observed only after 50 000 cycles. Conclusion. Based on these laboratory results, it is concluded that G-coat Plus is indicated in association with GP IX Extra with the aim to improve the mechanical properties of the former. However, this study is limited to a short-term observation.

11 November 2020 in BMC Oral Health
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MAMariana Pinheiro Araujo
Mariana Pinheiro Araujo
NINicola Patricia Innes
Nicola Patricia Innes
CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
Daniela HesseDaniela Hesse
Daniela Hesse
IOIsabel Cristina Olegário
Isabel Cristina Olegário
DRDaniela Raggio
Daniela Raggio
Background: Atraumatic Restorative Treatment (ART) and the Hall Technique (HT) are both minimally invasive, non-aerosol generating procedures (non-AGPs). They seem to have never been directly compared, nor has the HT been studied in a non-clinical setting. This study compared the HT and ART restorations placed in a school setting after 36 months. Methods: Children (5–10 yo) who had a primary molar with a dentinal occluso-proximal, cavitated carious lesion were allocated to the ART (selective removal) or HT arms. Primary outcome: restoration survival over 36-months (using Kaplan–Meier survival analysis, log rank test, and Cox regression). Secondary outcomes: (1) occlusal vertical dimension (OVD) (1, 2, 3, 4 weeks) and (2) child self-reported discomfort; (3) treatment acceptability (immediately following interventions); (4) Child Oral Health Related Quality of Life (OHRQoL), before treatment and after 6 months and (5) a post hoc analysis of time to tooth exfoliation (1, 6, 12, 18, 24, 30, 36 months). Results: One-hundred and thirty-one children (ART = 65; HT = 66) were included (mean age = 8.1 ± 1.2). At 36 months, 112 (85.5%) children were followed-up. Primary outcome: restoration survival rates ART = 32.7% (SE = 0.08; 95% CI 0.17–0.47); HT = 93.4% (0.05; 0.72–0.99), p < 0.001; Secondary outcomes: (1) OVD returned to pre-treatment state within 4 weeks; (2) treatment discomfort was higher for the HT (p = 0.018); (3) over 70% of children and parents showed a high acceptability for treatments, with crown aesthetics being a concern for around 23% of parents; (4) Child OHRQoL improved after 6 months; and (5) teeth treated with the HT exfoliated earlier than those in the ART group (p = 0.007). Conclusions: Both ART and the HT were acceptable to child participants and their parents and all parents thought both restorations protected their child’s tooth. However, the crown appearance concerned almost a quarter of parents in the HT arm. Children experienced less discomfort in the ART group. Although both treatments can be performed in a non-clinical setting and have the advantage of being non-aerosol generating procedures (non-AGPs), the HT had almost three times higher survival rates (93.4%) for restoring primary molar occluso-proximal cavities compared to ART (32.7%). Trial registration: This trial was registered in ClinicalTrials.gov (NCT02569047), 5th October 2015. https://clinicaltrials.gov/ct2/show/study/NCT02569047?cond=Hall+Technique+Atraumatic+Rest orative+Treatment&draw=2&rank=2.

31 March 2016 in Trials
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Daniela HesseDaniela Hesse
Daniela Hesse
MAMariana Pinheiro de Araujo
Mariana Pinheiro de Araujo
IOIsabel C Olegário
Isabel C Olegário
NINicola Innes
Nicola Innes
DRDaniela Raggio
Daniela Raggio
CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
In many parts of the world, school-age children have high dental treatment needs; however, there is often low, or no, dental care provision. Although Atraumatic Restorative Treatment (ART) was developed to address this, its survival rate in occluso-proximal lesions is low. An alternative, the Hall Technique (HT) has shown better relative outcomes for occluso-proximal lesions, but has not been directly compared to ART or tested in field settings. This trial will compare ART and the HT for the most clinically- and cost-effective strategy for managing occluso-proximal lesions in primary molars, in a school setting, using low-technology and child-friendly dental techniques. This two-arm, parallel group, patient-randomized controlled, superiority trial will have treatment provided in schools. Schoolchildren (n = 124, age 6–8) with at least one occluso-proximal carious primary molar lesion will have random allocation to treatment with ART or HT. Baseline measures and outcome data will be assessed through participant report, clinical examination and parent report/questionnaires. The primary outcome is survival rate, a composite measure of absence of Minor Failures (a defect in the restoration/crown, but not interfering with tooth health) and Major Failures (signs or symptoms of irreversible pulp damage, such as dental fistula/abscess, tooth fracture or failures that cannot be repaired). Secondary outcomes are: (1) child-reported discomfort, (2) childrens’ and (3) parents’ concerns around dental appearance and (4) acceptability of treatments, (5) occlusal-vertical dimensions (OVD) changes, (6) plaque index, (7) gingival health, (8) decayed, missing, filled teeth in permanent teeth (DMFT)/decayed, missing, filled teeth in primary teeth (dmft), (9) oral health-related-quality of life, reported by children and parents/caregivers, (10) the incremental cost-effectiveness, and (11) operator effect. A trained and calibrated examiner will evaluate the treated teeth after 1 week, then 1, 6, 12, 24 and 36 months post treatment. Kaplan-Meier and Cox regression tests will be used to investigate the primary outcome. The Mann-Whitney or t test, Friedman test, paired t test or Wilcoxon test and Ordinal Logistic Regression Analysis will be used to analyze the secondary outcomes. The results of this trial will support decision-making by clinicians and policy-makers for managing occluso-proximal lesions in settings with constrained resources and limited dental access. www.clinicaltrials.gov, NCT02569047 , registered 5 October 2015.

14 August 2012 in International Journal of Paediatric Dentistry
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CBClarissa Calil Bonifácio
Clarissa Calil Bonifácio
Daniela HesseDaniela Hesse
Daniela Hesse
DRDaniela Raggio
Daniela Raggio
MBMarcelo Bönecker
Marcelo Bönecker
CLCor Van Loveren
Cor Van Loveren
WAW Evert Van Amerongen
W Evert Van Amerongen