CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 240 enrolled
Drug / intervention
Standard 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.

Search/NCT02542943
NCT02542943N/ACompleted
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A Clinical Study Investigating the Efficacy of Two Experimental Oral Rinses in Providing Long Term Relief From Dentinal Hypersensitivity

GlaxoSmithKline·interventional·Posted Sep 7, 2015·Updated Mar 6, 2017

In Brief

A clinical study evaluating Experimental Oral Rinse 1, Experimental Oral Rinse 2, and 2 other interventions for Dentin Sensitivity. Completed, enrolled 240 participants across 1 site.

Detailed Summary

This study will investigate the longitudinal efficacy of two experimental oral rinses containing 1.5% weight/weight (w/w) dipotassium oxalate monohydride (KOX), formulated at pH 4.5 and pH 7 respectively, for the relief of dentinal hypersensitivity (DH), compared to a placebo oral rinse, when used as an adjunct to twice daily brushing with a standard fluoride toothpaste.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentin Sensitivity
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedSep 7, 2015
Enrollment StartSep 1, 2015
Primary CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 10.8 years ago

Interventions

Experimental Oral Rinse 1device

(1.5% w/w KOX, pH 4.5)

Experimental Oral Rinse 2device

(1.5% w/w KOX, pH 7)

Placebo Oral Rinseother

(0% w/w KOX, pH 4.5)

Standard fluoride toothpastedrug

1000ppm fluoride as sodium monofluorophosphate