At a glance
ClinicalIndex Comparison RecordN/ACompleted· 120 enrolled
Drug / intervention
Stannous fluoride toothpaste +3 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 Randomized Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity
In Brief
A clinical study evaluating Dipotassium oxalate toothpaste, Stannous fluoride toothpaste, and 2 other interventions for Dentin Hypersensitivity. Completed, enrolled 120 participants across 1 site.
Detailed Summary
The objective of this study is to evaluate the efficacy (changes in dentinal hypersensitivity) and safety (oral soft tissue evaluation) after use of one of four dentifrices in subjects with pre-existing hypersensitivity over an 11-week period.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Hypersensitivity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2020202120222023202420252026
First PostedMay 2019
Enrollment StartJul 2019
Primary CompletionOct 2019
TodayJul 2026
First PostedMay 28, 2019
Enrollment StartJul 8, 2019
Primary CompletionOct 3, 2019
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 7.1 years ago
Interventions
Dipotassium oxalate toothpastedevice
Experimental dipotassium oxalate (3%) toothpaste
Stannous fluoride toothpastedrug
Marketed stannous fluoride (0.454%) toothpaste
Potassium nitrate toothpastedrug
Marketed potassium nitrate (5%) toothpaste
Sodium monofluorophosphate toothpastedrug
Marketed sodium monofluorophosphate (0.76%) toothpaste