At a glance
ClinicalIndex Comparison RecordN/ACompleted· 488 enrolled
Drug / intervention
Stannous Fluoride dentifice +1 moredevice
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 clinical study evaluating Stannous Fluoride dentifice and Sodium Monofluorophosphate dentifrice for Dentin Sensitivity. Completed, enrolled 488 participants across 2 sites.
Detailed Summary
This single centre, dual site, 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
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Sensitivity
CountriesUnited Kingdom
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartNov 2015
First PostedNov 2015
Primary CompletionJun 2016
TodayJul 2026
First PostedNov 23, 2015
Enrollment StartNov 1, 2015
Primary CompletionJun 3, 2016
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 10.6 years ago
Interventions
Stannous Fluoride dentificedevice
Experimental dentifrice containing 0.454% w/w stannous fluoride (1100ppm)
Sodium Monofluorophosphate dentifriceother
Dentifrice containing 0.76% sodium monofluorophosphate (1000ppm fluoride)