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Meta-analysis of Stannous Fluoride and the Effects on Gingival Health

NCT03970759 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2890

Last updated 2019-06-17

No results posted yet for this study

Summary

The aim of this 18 study analysis was to compare the effect of bioavailable stannous fluoride (SnF2) dentifrices when used up to 3 months on gingivitis relative to a positive or negative control dentifrice.

Conditions

  • Gingivitis

Interventions

DRUG

Stannous Fluoride Dentifrice

Experimental stannous fluoride (0.454%) dentifrice

DRUG

Positive control dentifrice

Positive control dentifrice containing (0.3%) triclosan.

DRUG

Negative control dentifrice

Negative control dentifrice containing either sodium fluoride (0.243%) or sodium monofluorophosphate (0.76%)

Sponsors & Collaborators

  • Procter and Gamble

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-08
Primary Completion
2018-11-30
Completion
2018-11-30
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03970759 on ClinicalTrials.gov