Safety and efficacy of a nightguard bleaching agent containing sodium fluoride and potassium nitrate

William D. Browning, Daniel C.N. Chan, Kevin B. Frazier, Richard S. Callan, John S. Blalock

Research output: Contribution to journalArticle

27 Scopus citations

Abstract

Objectives: Transient sensitivity during bleaching is generally reported to affect 67% of patients. While most people tolerate this sensitivity, some find it impossible to continue treatment. The purpose of this study was to determine the safety and efficacy of an experimental, low-sensitivity bleaching agent. Method and materials: Twenty-two participants bleached for a minimum of 6 hours per night over a 2-week period. The bleaching agent used, Experimental Product E, is a 10% carbamide peroxide gel containing potassium nitrate and sodium fluoride. Evaluations were performed at baseline and 1, 2, 13, and 26 weeks. Color change was measured using a value-ordered Vita classic shade guide and a colorimeter. Sensitivity of the teeth, gingiva, tongue, and/or throat was measured daily using a patient log. Results: The median color change after 2 weeks was eight tabs. Approximately 36% reported sensitivity during the active whitening phase of the study. As a group, participants reported sensitivity during 13.7% of the total days spent whitening. Conclusion: Experimental Product E was shown to be safe. Participants experienced minor sensitivity during the active bleaching phase only. Experimental Product E was shown to be an effective bleaching agent for the subjects tested in this study.

Original languageEnglish (US)
Pages (from-to)693-698
Number of pages6
JournalQuintessence international
Volume35
Issue number9
StatePublished - Oct 1 2004

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Keywords

  • 10% carbamide peroxide
  • Colorimeter
  • Double-blind clinical trial
  • Efficacy
  • Human subject
  • Potassium nitrate
  • Safety
  • Sensitivity
  • Tooth bleaching
  • Vita shade guide

ASJC Scopus subject areas

  • Dentistry(all)

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