Randomized clinical trials in periodontology: focus on outcomes selection

dc.creatorClaúdio Mendes Pannuti
dc.creatorFernando de Oliveira Costa
dc.creatorNathalia Vilela Souza
dc.creatorBelen Retamal-Valdes
dc.creatorAmanda Almeida Costa
dc.creatorCristiano Susin
dc.creatorMagda Feres
dc.date.accessioned2024-07-02T17:34:33Z
dc.date.accessioned2025-09-09T00:01:47Z
dc.date.available2024-07-02T17:34:33Z
dc.date.issued2021-09-24
dc.identifier.doihttps://doi.org/10.1590/1807-3107bor-2021.vol35.0100
dc.identifier.issn1807-3107
dc.identifier.urihttps://hdl.handle.net/1843/69592
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofBrazilian Oral Research
dc.rightsAcesso Aberto
dc.subjectTreatment outcome
dc.subjectPeriodontics
dc.subjectRandomized controlled trial
dc.subject.otherClinical trials
dc.subject.otherperiodontology
dc.subject.otherperiodontal outcomes
dc.titleRandomized clinical trials in periodontology: focus on outcomes selection
dc.typeArtigo de periódico
local.citation.epage9
local.citation.issueSuppl 2
local.citation.spage1
local.citation.volume35
local.description.resumoRandomized clinical trials (RCTs) are human studies carried out to compare different treatments or interventions, and their results are used to support clinical decision-making and improve patient care. Herein, the aim of this study was to review the selection process of study outcomes in periodontology. Primary outcomes should draw the main conclusions of the study, whereas secondary outcomes should only be used to help explain the main findings and generate future research hypothesis. Outcomes are classified as clinically relevant (CROs) or surrogate outcomes. CROs – the first option for primary outcome variables - should convey not only substantial health benefits, but also be deemed important by patients. In periodontology, tooth loss/retention and oral health–related quality of life (OHRQoL) are examples of CROs. While tooth loss has main limitations as a primary outcome, emerging evidence suggest that patient-reported outcome measures (PROMs) can accurately detect OHRQoL following periodontal therapy. When CROs cannot be assessed, validated surrogate outcomes can be used as proxies. Primary outcome variables should reflect a treatment endpoint at the patient level that can be easily used to inform decision-making in daily practice. These outcomes should allow the implementation of a treat-to-target concept in which the intervention can be clearly judged against a prespecified treatment target. Recently, the presence of at most 4 sites with periodontal probing depth ≥5 mm post-treatment was suggested as an effective endpoint for periodontal trials. In perspective, a combination of validated clinical parameters and PROMs will provide a more comprehensive assessment of periodontal treatments.
local.identifier.orcidhttps://orcid.org/0000-0003-4181-3975
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICA
local.publisher.initialsUFMG
local.url.externahttps://www.scielo.br/j/bor/a/Q8BYsndhvc5h5Gdnm99yKvC/?lang=en

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