Postoperative sensitivity in posterior resin composite restorations with prior application of a glutaraldehyde-based desensitizing solution: a randomized clinical trial

2021 ◽  
pp. 103918
Author(s):  
Isabelle Lins Macêdo de Oliveira ◽  
Taíse Alessandra Hanzen ◽  
Alexandra Mara de Paula ◽  
Jorge Perdigão ◽  
Marcos Antonio Japiassú Resende Montes ◽  
...  
2016 ◽  
Vol 10 (01) ◽  
pp. 016-022 ◽  
Author(s):  
Hande Kemaloglu ◽  
Tijen Pamir ◽  
Huseyin Tezel

ABSTRACT Objective: To compare the performance and postoperative sensitivity of a posterior resin composite with that of bonded amalgam in 40 (n = 20) large sized cavities and to evaluate whether resin composite could be an alternative for bonded amalgam. Materials and Methods: This was a randomized clinical trial. Twenty patients in need of at least two posterior restorations were recruited. Authors randomly assigned one half of the restorations to receive bonded amalgam and the other half to composite restorations. Forty bonded amalgams (n = 20) and composites (n = 20) were evaluated for their performance on modified-US Public Health Service criteria and postoperative sensitivity using visual analogue scale (VAS) for 36-months. Results: Success rate of this study was 100%. First clinical alterations were rated as Bravo after 1 year in marginal discoloration, marginal adaptation, anatomical form, and surface roughness for both amalgam and composite. At the 3rd year, overall “Bravo” rated restorations were 12 for bonded amalgam and 13 for resin composites. There were no significant differences among the VAS scores of composites and bonded amalgams for all periods (P > 0.05) except for the comparisons at the 3rd year evaluation (P < 0.05). Conclusions: Within the limitation of this study, both resin composite and bonded amalgam were clinically acceptable. Postoperative sensitivity results tend to decrease more in composite restorations rather than amalgams. Therefore, it was concluded that posterior resin composite can be used even in large sized cavities.


2009 ◽  
Vol 34 (6) ◽  
pp. 648-655 ◽  
Author(s):  
M. F. Burrow ◽  
D. Banomyong ◽  
C. Harnirattisai ◽  
H. H. Messer

Clinical Relevance Glass-ionomer lining showed no benefit in reducing postoperative sensitivity associated with occlusal resin composite restorations. The use of self-etching adhesive demonstrated postoperative sensitivity similar to that of total-etching adhesive.


ORL ro ◽  
2018 ◽  
Vol 4 (41) ◽  
pp. 45
Author(s):  
Irina-Maria Gheorghiu ◽  
Loredana Mitran ◽  
Mihai Mitran ◽  
Anca-Nicoleta Temelcea ◽  
Sânziana Scărlătescu ◽  
...  

2020 ◽  
Vol 45 (5) ◽  
pp. 473-483 ◽  
Author(s):  
CAGA Costa ◽  
NLG Albuquerque ◽  
JS Mendonça ◽  
AD Loguercio ◽  
VPA Saboia ◽  
...  

Clinical Relevance At 24 months, the dentin pretreatment with epigallocatechin-3-gallate did not impair the clinical performance of the adhesive Single Bond Universal regardless of the bonding strategy used. SUMMARY Purpose: To evaluate the two-year effect of dentin pretreatment with epigallocatechin-3-gallate (EGCG) on the clinical performance of restorations of noncarious cervical lesions (NCCLs) with Single Bond Universal, applied in two different modes (self-etch and etch-and-rinse). Methods and Materials: In this randomized clinical trial, 33 volunteers were selected, and 156 NCCLs were assigned to four groups: ER, etch-and-rinse; ER-EGCG, 0.1% EGCG dentin pretreatment + etch-and-rinse; SE, self-etch; and SE-EGCG, 0.1% EGCG dentin pretreatment + self-etch. The NCCLs were restored with a nanofilled resin composite and evaluated at baseline and at six, 12, 18, and 24 months using FDI criteria for retention, marginal staining, marginal adaptation, caries, and postoperative sensitivity. Two evaluators were blinded to the treatments performed, and impressions were taken for resin replicas to allow indirect observations. Statistical analyses were performed with Kruskal-Wallis and McNemar tests with a significance level of 5%. Results: Six restorations (one from ER, two from SE, one from ER-EGCG, and two from SEEGCG) were lost at 24 months with no significant differences (p&gt;0.05). The retention rates were 97.0% (ER and ER-EGCG), 94.1% (SE), and 94.2% (SE-EGCG). For marginal adaptation, a significant difference was detected between the baseline and 24 months for the SE group (p=0.0313). There were no statistical differences among all other evaluated criteria at 24 months, neither for each group at baseline nor for 24-month comparisons (p&gt;0.05). Conclusions: The pretreatment with EGCG provided no benefit in the clinical performance of the adhesive regardless of the bonding strategy used. In addition, it adds an additional required step to the restorative procedure.


1998 ◽  
Vol 26 (7) ◽  
pp. 555-562 ◽  
Author(s):  
N.J.M Opdam ◽  
F.J.M Roeters ◽  
A.J Feilzer ◽  
E.H Verdonschot

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