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Evaluation of a Low-fluoride Anticaries Toothpaste

Completed
Conditions
Tooth Abnormality
Interventions
Drug: Fluorides, Topical
Registration Number
NCT01094210
Lead Sponsor
Indiana Nanotech, LLC
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • 30 adult subjects (between 18-50 years of age)
Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
G1Fluorides, Topical500 ppm F Test Toothpaste
G2Fluorides, Topical1100 ppm F Control Toothpaste
Primary Outcome Measures
NameTimeMethod
Transverse Microradiography30 days

X-ray analysis of enamel lesion

Surface Microhardness30 days

Strength measurements made at the enamel surface of the enamel specimen

Cross-Sectional Microhardness30 days

Strength measurements made within the enamel lesion of the enamel specimen

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dental Diagnostic Clinic within the University of Texas Health Science Center

🇺🇸

San Antonio, Texas, United States

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