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To Investigate the Gingivitis Efficacy of a Stannous Fluoride Dentifrice in a Chinese Population

Gingivitis Clinical Trial

Official title:
A Clinical Study Investigating the Gingivitis Efficacy of a Stannous Fluoride Dentifrice in a Chinese Population.

Clinical Trial Summary

This single-centre, examiner-blind, randomized, stratified, two-treatment, parallel group clinical study will evaluate the efficacy of a 0.454% w/w stannous fluoride dentifrice compared to a reference dentifrice to control gingivitis (gingival bleeding and visual signs of gingival inflammation) in dentally and periodontally healthy adult volunteers over 12 weeks use in a Chinese population.

Clinical Trial Description

This clinical study will be carried out in healthy adult volunteers with moderate gingivitis. Treatment effect will be determined by evaluating the efficacy, in a Chinese population, of a dentifrice containing 0.454% w/w stannous fluoride to control gingivitis and supra-gingival plaque following 6 and 12 weeks twice daily brushing, compared to a fluoride control dentifrice. During the 12 week treatment period, participant will brush with their allocated study product twice daily. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02937636
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase N/A
Start date September 19, 2017
Completion date December 22, 2017
View Details
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