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Supplemental vibrational force does not reduce pain experience during initial alignment with fixed orthodontic appliances: a multicenter randomized clinical trial.
Woodhouse, Neil R; DiBiase, Andrew T; Papageorgiou, Spyridon N; Johnson, Nicola; Slipper, Carmel; Grant, James; Alsaleh, Maryam; Cobourne, Martyn T.
Afiliação
  • Woodhouse NR; King's College London Dental Institute, Department of Orthodontics, London SE19RT, UK.
  • DiBiase AT; Brighton and Sussex University Hospitals NHS Foundation Trust, Royal Alexandra Children's Hospital, Department of Orthodontics, Brighton BN25BE, UK.
  • Papageorgiou SN; East Kent Hospitals University NHS Foundation Trust, William Harvey Hospital, Department of Orthodontics, Ashford TN240LZ, UK.
  • Johnson N; University of Bonn, Department of Orthodontics and Department of Oral Technology, Bonn DE-53111, Germany.
  • Slipper C; Brighton and Sussex University Hospitals NHS Foundation Trust, Royal Alexandra Children's Hospital, Department of Orthodontics, Brighton BN25BE, UK.
  • Grant J; Brighton and Sussex University Hospitals NHS Foundation Trust, Royal Alexandra Children's Hospital, Department of Orthodontics, Brighton BN25BE, UK.
  • Alsaleh M; Brighton and Sussex University Hospitals NHS Foundation Trust, Royal Alexandra Children's Hospital, Department of Orthodontics, Brighton BN25BE, UK.
  • Cobourne MT; King's College London Dental Institute, Department of Orthodontics, London SE19RT, UK.
Sci Rep ; 5: 17224, 2015 Nov 27.
Article em En | MEDLINE | ID: mdl-26610843
This prospective randomized trial investigated the effect of supplemental vibrational force on orthodontic pain during alignment with fixed-appliances. Eighty-one subjects < 20 years-old undergoing extraction-based fixed-appliance treatment were randomly allocated to supplementary (20-minutes/day) use of an intra-oral vibrational device (AcceleDent(®)) (n = 29); an identical non-functional (sham) device (n = 25) or fixed-appliances only (n = 27). Each subject recorded pain intensity (using a 100-mm visual-analogue scale) and intake of oral analgesia in a questionnaire, following appliance-placement (T1) and first-adjustment (T2) for 1-week (immediately-after, 4, 24, 72-hours and at 1-week). Mean maximum-pain for the total sample was 72.96 mm [SD 21.59; 95%CI 68.19-77.74 mm] with no significant differences among groups (P = 0.282). Subjects taking analgesics reported slightly higher maximum-pain although this was not significant (P = 0.170). The effect of intervention was independent of analgesia (P = 0.883). At T1 and T2, a statistically and clinically significant increase in mean pain was seen at 4 and 24-hours, declining at 72-hours and becoming insignificant at 1-week. For mean alignment-rate, pain-intensity and use of analgesics, no significant differences existed between groups (P > 0.003). The only significant predictor for mean pain was time. Use of an AcceleDent vibrational device had no significant effect on orthodontic pain or analgesia consumption during initial alignment with fixed appliances.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Medição da Dor / Braquetes Ortodônticos Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Dor / Medição da Dor / Braquetes Ortodônticos Tipo de estudo: Clinical_trials / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Female / Humans / Male Idioma: En Ano de publicação: 2015 Tipo de documento: Article