NCT03310268 - A Clinical Study to Evaluate a Stannous Fluoride Toothpaste for the Relief of Dentinal Hypersensitivity | Biotech Hunter

Enrollment

185

Participants

Timeline

Start Date

November 18, 2017

Primary Completion Date

February 2, 2018

Study Completion Date

February 2, 2018

Conditions

Dentin Sensitivity

Interventions

OTHER

0.454% Stannous fluoride (SnF2) and 0.072% sodium fluoride (NaF): 1450 ppm fluoride in total

Participants will be instructed to apply experimental dentifrice (containing 454% SnF2 and 0.072% NaF, 1450 ppm fluoride in total), covering the full length of toothbrush head (full ribbon) and will brush twice daily (morning and evening) for one timed minute (in their usual manner) and expectorate.

OTHER

1400 ppm fluoride as sodium monofluorophosphate (SMFP)

Participants will be instructed to apply negative control dentifrice (containing 1400 ppm fluoride as SMFP), covering the full length of toothbrush head (full ribbon) and will brush twice daily (morning and evening) for one timed minute (in their usual manner) and expectorate.

OTHER

Stannous Chloride (SnCl2) and 0.15% NaF: 1450 ppm fluoride in total

Participants will be instructed to apply positive control dentifrice (containing SnCl2 and 0.15% NaF, 1450 ppm fluoride in total), covering the full length of toothbrush head (full ribbon) and will brush twice daily (morning and evening) for one timed minute (in their usual manner) and expectorate.

Trial Locations (1)

200023

GSK Investigational Site, Shanghai