Clinical Trials Directory

Trials / Completed

CompletedNCT07419737

Dental Plaque Prevention Efficacy of a Stannous Fluoride Toothpaste

Dental Plaque Prevention Efficacy Evaluation and Comparison of a Stannous Fluoride Toothpaste

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
91 (actual)
Sponsor
Church & Dwight Company, Inc. · Industry
Sex
All
Age
18 Years – 69 Years
Healthy volunteers
Accepted

Summary

This randomized, stratified, double-blind, two-cell parallel clinical study evaluated the dental plaque prevention efficacy of a stannous fluoride toothpaste compared to a sodium fluoride control toothpaste following a professional dental prophylaxis. Adult subjects brushed twice daily for 14 days with their assigned dentifrice. Plaque was assessed using the Lobene-Soparkar modification of the Turesky Modification of the Quigley-Hein Plaque Index at baseline, Day 1, and Day 14 following periods of oral hygiene abstention.

Detailed description

This two-week, randomized, double-blind, parallel-group study evaluated plaque prevention following dental cleaning. Subjects meeting plaque qualification criteria underwent a complete prophylaxis and were randomized to either a stannous fluoride test dentifrice or a sodium fluoride control dentifrice. Subjects brushed twice daily for two minutes with the assigned product. Plaque accumulation was assessed at baseline, after one day of use, and after 14 days of use following overnight abstention from oral hygiene. Plaque was disclosed and scored on facial and lingual tooth surfaces using the Lobene-Soparkar modified Turesky Plaque Index. Treatment comparisons were performed using ANCOVA with baseline plaque as a covariate.

Conditions

Interventions

TypeNameDescription
DRUGStannous Fluoride Toothpaste (SnF)Test toothpaste (0.454% SnF)
DRUGSodium Fluoride DentifriceComparator toothpaste (0.243% NaF)

Timeline

Start date
2024-10-16
Primary completion
2024-12-04
Completion
2024-12-04
First posted
2026-02-19
Last updated
2026-02-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07419737. Inclusion in this directory is not an endorsement.