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Trials / Withdrawn

WithdrawnNCT02708160

Assessment of Prevident Sodium Fluoride 1.1% Toothpaste Using an Intra-oral Remineralization-demineralization Model

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Colgate Palmolive · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

This is a double blind, cross-over, controlled clinical trial utilizing thirty (30) adults to evaluate remineralization of early caries lesions.

Conditions

Interventions

TypeNameDescription
DRUGFluoride Free toothpasteBrush whole mouth with study toothpaste 2x/day for the 2 week test period. Each brushing routine is 1 minute whole mouth brushing with oral retainer in mouth, spit out toothpaste residue and wait 1 minute before rinsing with water.
DRUG1.1% Fluoride toothpasteBrush whole mouth with study toothpaste 2x/day for the 2 week test period. Each brushing routine is 1 minute whole mouth brushing with oral retainer in mouth, spit out toothpaste residue and wait 1 minute before rinsing with water.
DRUG0.243% Fluoride toothpasteBrush whole mouth with study toothpaste 2x/day for the 2 week test period. Each brushing routine is 1 minute whole mouth brushing with oral retainer in mouth, spit out toothpaste residue and wait 1 minute before rinsing with water.

Timeline

Start date
2016-03-01
Primary completion
2016-06-01
Completion
2016-06-01
First posted
2016-03-15
Last updated
2019-02-21

Source: ClinicalTrials.gov record NCT02708160. Inclusion in this directory is not an endorsement.

Assessment of Prevident Sodium Fluoride 1.1% Toothpaste Using an Intra-oral Remineralization-demineralization Model (NCT02708160) · Clinical Trials Directory