Clinical Trials Directory

Trials / Completed

CompletedNCT04006470

Meta-analysis of Stannous Fluoride and the Effects on Enamel Erosion

Bioavailable Stannous Fluoride Dentifrice Meta-Analyses: Effects on Dentine Hypersensitivity and Enamel Erosion

Status
Completed
Phase
Study type
Observational
Enrollment
172 (actual)
Sponsor
Procter and Gamble · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this 5 study analysis was to compare the effect of bioavailable stannous fluoride (SnF2) dentifrices to assess enamel erosion protection in-situ using surface profilometry.

Conditions

Interventions

TypeNameDescription
DRUGStannous fluoride dentifriceStannous fluoride (0.454%) dentifrice
DRUGPositive control dentifricePositive control dentifrice containing potassium nitrate or arginine.
DRUGNegative control dentifriceNegative control dentifrice containing either sodium fluoride (0.243%) or sodium monofluorophosphate (0.76%)

Timeline

Start date
2018-01-08
Primary completion
2018-11-30
Completion
2018-11-30
First posted
2019-07-05
Last updated
2019-07-05

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04006470. Inclusion in this directory is not an endorsement.