At a glance
ClinicalIndex Comparison RecordN/ACompleted· 56 enrolled
Drug / intervention
Sodium Fluoride +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Placebo Controlled Study to Evaluate the Effectiveness of Experimental Foaming Gel Toothpastes Using an In-situ Erosion Remineralization Model
In Brief
A clinical study evaluating Sodium Fluoride and Potassium nitrate for Dental Erosion and Acid Wear. Completed, enrolled 56 participants across 1 site.
Detailed Summary
The purpose of this study is to compare and evaluate the ability of two European Union (EU) regulated gel to foam toothpaste formulations versus a non-fluoride toothpaste using a modified in-situ model of dental erosion and remineralization. A positive control i.e fluoride containing toothpaste marketed in EU will also be compared to non-fluoride toothpaste.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDental Erosion, Acid Wear
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartNov 2011
Primary CompletionFeb 2012
First PostedAug 2012
TodayJul 2026
First PostedAug 6, 2012
Enrollment StartNov 1, 2011
Primary CompletionFeb 1, 2012
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 13.9 years ago
Interventions
Sodium Fluoridedrug
Toothpaste containing 1450 ppm F - EU level as NaF.
Potassium nitratedrug
All study treatments contain 5% w/w KNO3.