At a glance
ClinicalIndex Comparison RecordN/ACompleted· 221 enrolled
Drug / intervention
Experimental Oral Rinse 1 (1.5% w/w KOX, 0ppm F, pH 7.0) +2 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 Two Experimental Oral Rinses in Providing Long Term Relief From Dentinal Hypersensitivity
In Brief
A clinical study evaluating Experimental Oral Rinse 1 (1.5% w/w KOX, 0ppm F, pH 7.0), Experimental Oral Rinse 2 (2.0% w/w KOX, 45ppm F, pH 4.5), and 1 other intervention for Dentin Sensitivity. Completed, enrolled 221 participants across 1 site.
Detailed Summary
This will be a single center, eight week, randomized, double blind, three treatment arm, parallel design, stratified (by mean baseline Schiff Sensitivity Score of the two selected test teeth) study in healthy participants.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Sensitivity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartJan 2016
First PostedJan 2016
Primary CompletionApr 2016
Study CompletionApr 2016
TodayJul 2026
First PostedJan 11, 2016
Enrollment StartJan 4, 2016
Primary CompletionApr 1, 2016
Study CompletionApr 22, 2016
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 10.5 years ago
Interventions
Experimental Oral Rinse 1 (1.5% w/w KOX, 0ppm F, pH 7.0)other
1.5% w/w KOX, 0ppm F, pH 7.0
Experimental Oral Rinse 2 (2.0% w/w KOX, 45ppm F, pH 4.5)other
2.0% w/w KOX, 45ppm F, pH 4.5
Placebo Oral Rinse (0% w/w KOX 0ppm F, pH 4.5 )other
0% w/w KOX 0ppm F, pH 4.5