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

NCT04006470 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 172

Last updated 2019-07-05

No results posted yet for this study

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

  • Enamel Erosion

Interventions

DRUG

Stannous fluoride dentifrice

Stannous fluoride (0.454%) dentifrice

DRUG

Positive control dentifrice

Positive control dentifrice containing potassium nitrate or arginine.

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 NCT04006470 on ClinicalTrials.gov