At a glance
ClinicalIndex Comparison RecordPhase 4Completed· 229 enrolled
Drug / intervention
stannous fluoride +1 moreother
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 Clinical Study Investigating the Efficacy of an Occluding Dentifrice in Providing Relief From Dentinal Hypersensitivity
In Brief
A Phase 4 clinical trial evaluating stannous fluoride and sodium monofluorophosphate for Dentin Sensitivity. Completed, enrolled 229 participants across 1 site.
Detailed Summary
This single centre, comparative design study will be used to investigate the efficacy of an experimental stannous fluoride containing dentifrice in relieving dentinal hypersensitivity (DH) after short term use compared with a standard fluoride dentifrice
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Sensitivity
CountriesCanada
Collaborators--
Timeline
Phase 4CompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartApr 2016
First PostedApr 2016
Primary CompletionMay 2016
Study CompletionMay 2016
TodayJul 2026
First PostedApr 8, 2016
Enrollment StartApr 1, 2016
Primary CompletionMay 1, 2016
Study CompletionMay 20, 2016
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 10.2 years ago
Interventions
stannous fluorideother
0.454% weight by weight (w/w) stannous fluoride containing 1100ppm fluoride
sodium monofluorophosphateother
0.76% w/w sodium monofluorophosphate containing 1000ppm fluoride