Effect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trial

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dc.creatorGustavo Henrique Mattos Pereira
dc.creatorRafael Paschoal Esteves Lima
dc.creatorLuis Otávio de Miranda Cota
dc.creatorFernando de Oliveira Costa
dc.date.accessioned2024-05-24T19:04:46Z
dc.date.accessioned2025-09-08T23:21:51Z
dc.date.available2024-05-24T19:04:46Z
dc.date.issued2020-01-01
dc.identifier.doihttps://doi.org/10.4317%2Fmedoral.56171
dc.identifier.issn19895488
dc.identifier.urihttps://hdl.handle.net/1843/68597
dc.languageeng
dc.publisherUniversidade Federal de Minas Gerais
dc.relation.ispartofJournal of Clinical and Experimental Dentistry
dc.rightsAcesso Aberto
dc.subjectAnalgesia
dc.subjectDental implants
dc.subjectIbuprofen
dc.subjectPain measurement
dc.subjectPlacebos
dc.subject.otherpreemptive analgesia
dc.subject.otheribuprofen acesso open busca dia 23/05/2024Effect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trial
dc.subject.otherimplat surgery Journal of clinical and experimental dentistry
dc.subject.otherpain fao clínica busca dia 23/05/2024Effect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trial
dc.titleEffect of preemptive analgesia with ibuprofen in the control of postoperative pain in dental implant surgeries: a randomized, triple-blind controlled clinical trial
dc.typeArtigo de periódico
local.citation.epagee78
local.citation.issue1
local.citation.spagee71
local.citation.volume12
local.description.resumoPreemptive analgesia has as its basic principle the administration of analgesics before the onset of painful stimuli, in order to reduce or prevent postoperative pain, but this question is little explored in implantology. Thus, this study was conducted in order to evaluate the clinical efficacy of ibuprofen in pain prevention after unit implant surgery. Material and Methods For this triple-blind, parallel, placebo-controlled and randomized clinical trial, 54 insertion surgeries of unitary implants were performed. Two groups have received two different protocols 1 hour before surgery: Ibuprofen group (IBU) 600 mg of ibuprofen; and (2) placebo group (maize starch). The intensity of the pain was evaluated through the visual analogue scale (VAS) in 6 times (1, 6, 12, 24, 48 and 72 hours after the surgery). Patients were instructed to take 750 mg of paracetamol as rescue medication, if necessary. The occurrence and the intensity of pain were analyzed by means of an analysis of variance ANOVA with repeated measurements using the general linear model procedure. Results The IBU group had significantly lower VAS scores overall (IBU = 0.30, ± 0.57; placebo = 1.14, ± 1.07; p<0.001) and at all times in the intra, intergroup comparisons and time/group interaction than the placebo group (p<0.001). The use of rescue medication was significantly lower and the postoperative time was longer in the IBU group compared to placebo (p = 0.002). Conclusions The single use of ibuprofen was found to be significantly superior in reducing pain after unit implant surgery compared to placebo.
local.publisher.countryBrasil
local.publisher.departmentFAO - DEPARTAMENTO DE CLÍNICA
local.publisher.initialsUFMG
local.url.externahttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6969969/

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