Prolonged polymerization of a universal adhesive in non-carious cervical lesions: 36-month double-blind randomized clinical trial
| dc.coverage | DOI: 10.1016/j.jdent.2023.104823 | |
| dc.creator | Ñaupari-Villasante, Romina | |
| dc.creator | de Freitas, André | |
| dc.creator | Hass, Viviane | |
| dc.creator | Matos, Thalita P. | |
| dc.creator | Parreiras, Sibelli O. | |
| dc.creator | Reis, Alessandra | |
| dc.creator | Gutiérrez, Mario F. | |
| dc.creator | Loguercio, Alessandro D. | |
| dc.date | 2024 | |
| dc.date.accessioned | 2025-11-18T19:49:36Z | |
| dc.date.available | 2025-11-18T19:49:36Z | |
| dc.description | <p>Objective: To evaluate the effect of prolonged (P) polymerization time of a universal adhesive system applied in etch-and-rinse (ER) or self-etch (SE) strategies on the clinical performance of restorations in non-carious cervical lesions (NCCLs), after 36 months of clinical service. Methods: A total of 140 restorations were randomly placed in 35 subjects according to the polymerization time groups: ER (10 s); ER-P (40 s); SE (10 s); and SE-P (40 s) at 1,200 mW/cm<sup>2</sup>. Composite resin was placed incrementally. The restorations were evaluated immediately and after 6, 12, 18, and 36 months using the FDI criteria. Data were analyzed using the Kaplan-Meier survival test for retention loss, and the Kruskal-Wallis’ test for secondary outcomes (α = 0.05). Results: After 36 months, 19 restorations were lost: ER 6, ER-P 2, SE 9, SE-P 2. The retention rates were 82.3% for ER; 94.1 % for ER-P; 73.5 % for SE; and 94.1 % for SE-P, with a significant difference between ER vs. ER-P and SE vs. SE-P, as well as ER vs. SE-P and ER-P vs. SE (p < 0.0001). Minor defects were observed in 18 restorations for the marginal staining criteria: ER 5, ER-P 2, SE 8, SE-P 3; and in 33 restorations for the marginal adaptation criteria: ER 11, ER-P 4, SE 12, and SE-P 6 (p > 0.05). No restorations showed recurrence of caries or postoperative sensitivity. Conclusions: A prolonged polymerization time of 40 s improves the clinical performance of the universal adhesive for both adhesive strategies evaluated, even after 36 months. Clinical significance: Prolonging the polymerization time of a universal adhesive from 10 to 40 s has been shown to improve its clinical performance when used in NCCLs.</p> | eng |
| dc.identifier | https://investigadores.uandes.cl/en/publications/71b33df9-7ee0-4c94-8a24-b51feac400fc | |
| dc.identifier.uri | https://repositorio.uandes.cl/handle/uandes/56180 | |
| dc.language | eng | |
| dc.rights | info:eu-repo/semantics/restrictedAccess | |
| dc.source | vol.142 (2024) p.1-10 | |
| dc.subject | Clinical trial | |
| dc.subject | Non-carious cervical lesion | |
| dc.subject | Prolonged polymerization time | |
| dc.subject | Universal adhesive system | |
| dc.title | Prolonged polymerization of a universal adhesive in non-carious cervical lesions: 36-month double-blind randomized clinical trial | eng |
| dc.type | Article | eng |
| dc.type | Artículo | spa |