At a glance
ClinicalIndex Comparison RecordN/ACompleted· 655 enrolled
Drug / intervention
Potassium Nitrate + Sodium Fluorideother
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 Real-World Evidence Study Evaluating Oral Health Related Quality of Life Following the Use of Antisensitivity Toothpaste for Dentine Hypersensitivity Management
In Brief
A clinical study evaluating Potassium Nitrate + Sodium Fluoride for Dentin Sensitivity. Completed, enrolled 655 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate changes in oral health-related quality of life (OHrQoL) in participants suffering from Dentinal Hypersensitivity (DH) symptoms following the use of anti-sensitivity toothpaste for 24 weeks.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Sensitivity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedJul 2021
Enrollment StartAug 2021
Primary CompletionMay 2022
TodayJul 2026
First PostedJul 15, 2021
Enrollment StartAug 31, 2021
Primary CompletionMay 13, 2022
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 5.0 years ago
Interventions
Potassium Nitrate + Sodium Fluorideother
Potassium Nitrate 5% weight/weight (w/w) and Sodium Fluoride 0.15% weight/volume (w/v) fluoride ion.