A Clinical Method Development Study to Characterise The Efficacy of a Dentifrice For The Relief Of Dentin Hypersensitivity
Status:
Withdrawn
Trial end date:
2018-12-03
Target enrollment:
Participant gender:
Summary
The aim of this study is to develop the clinical methodology to characterize the efficacy
profiles of an experimental 5% potassium nitrate (KNO3) and 0.454% stannous fluoride (SnF2)
combination dentifrice and a marketed desensitizing 0.454% SnF2 only dentifrice for the
relief of dentin hypersensitivity (DH), at multiple time points, over an 8 week treatment
period.