Abstract
Objective
To compare 2 different resin composites and 2 adhesive systems used in a new restorative protocol (partial restoration) to treat non-carious cervical lesions associated with gingival recession type 1 (RT1).
Material and methods
Eighty combined defects (CDs) were treated with a partial restoration and periodontal plastic surgery for root coverage. The CDs were randomly assigned to one of the following groups: NP + TE (n = 20), nanofilled composite and 2-step total-etch adhesive system; NP + UA (n = 20), nanofilled composite and universal adhesive system; MH + TE (n = 20), microhybrid composite and 2-step total-etch adhesive; MH + UA (n = 20), microhybrid composite and universal adhesive. Restorations were assessed using the United States Public Health Service (USPHS) criteria at 1 week (baseline) and 6, 12, and 24 months. Survival rate, periodontal parameters, dentin hypersensitivity (DH), and aesthetics were also evaluated.
Results
After 24 months, only the MH + TE group did not lose any restoration, with no significant differences between groups. For surface roughness parameter, MH presented 83.3% of the restorations scoring Bravo, whereas NP presented 48.5% of the restorations scoring Bravo. All groups presented restorations with marginal discoloration. All periodontal parameters behaved similarly, regardless of the restorative material. All groups presented significant reductions of dentin hypersensitivity and improved aesthetic perceptions (p < 0.05).
Conclusion
Both resin composites and adhesives tested can be combined for partial restorations to treat CDs.
Clinical relevance
This new restorative-surgical protocol to treat CDs presents satisfactory outcomes. The partial restorations can be successfully executed with both combinations of adhesives and resin composites evaluated in this investigation.
TRN
ClinicalTrial.gov: NCT03215615; registration date July 12, 2017.
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Data availability
Data availability is upon request to the corresponding author.
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Acknowledgements
The authors would like to thank the Ultradent Inc. for the Valo light curing unit donated to Dr. Mathias-Santamaria.
Funding
Dr. Mathias-Santamaria was supported by the Coordination for the Improvement of Higher Education Personnel (CAPES), Brazil-Finance Code 001. Dr. Mauro Santamaria is supported by the National Council for Scientific and Technological Development from Brazil, CNPq (grant # 304269/2019–0).
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I.F.M.S. and M.P.S. were the coordinators of the study, created the study design and funding, performed all restorative and surgical procedures, and supervised all stages of the research. E.B. and C.A.S. performed clinical evaluations and collected the data. I.F.M.S. and C.A.S supported the patients with the necessary procedures during and after the trial. M.G.A. and G.S.A. assisted in the procedures. I.F.M.S., M.P.S., and E.B. wrote the main manuscript text. A.C.M., F.C.M., J.F.R., and M.A.S.M. revised the manuscript. All authors reviewed and approved the submission of the manuscript.
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All the treatment procedures were conducted according to the principles outlined in the Declaration of Helsinki and Ethical Conduct for Research with Human Beings and the Good Clinical Practice Guidelines. Written informed consent was taken from all participants included in the study.
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Mathias-Santamaria, I.F., Santamaria, M.P., Silveira, C.A. et al. Evaluation of a novel restorative protocol to treat non-carious cervical lesion associated with gingival recession: a 2-year follow-up randomized clinical trial. Clin Oral Invest 27, 1781–1792 (2023). https://doi.org/10.1007/s00784-022-04806-1
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DOI: https://doi.org/10.1007/s00784-022-04806-1