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Evaluation of a Low-fluoride Anticaries Toothpaste

NCT01094210 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2015-03-25

No results posted yet for this study

Summary

The purpose of this trial is to evaluate the anticaries remineralizing potential of a toothpaste containing 500 ppm fluoride plus fTCP technology relative to a commercially available toothpaste via a double-blind cross-over in situ (or intra-oral) clinical model, whereby approved human participants will wear an orthodontic appliance fitted with an enamel specimen for the duration of a leg (28 days). There will be two test legs.

Conditions

  • Tooth Abnormality

Interventions

DRUG

Fluorides, Topical

500 ppm F and 1100 ppm F topical toothpastes comprise sodium fluoride in each.

Sponsors & Collaborators

  • The University of Texas Health Science Center at San Antonio

    collaborator OTHER

  • Indiana Nanotech, LLC

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2011-03-31
Completion
2011-03-31

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 NCT01094210 on ClinicalTrials.gov