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Clinical Trial Summary

This will be a single centre, two week, randomised, examiner blind, two treatment arm, parallel design, stratified (by maximum baseline Schiff sensitivity score of the two selected test teeth), controlled study, in participant with at least two sensitive teeth that meet the study criteria at the Screening and Baseline visits. The study will be conducted in participants in good general health, with pre-existing self-reported and clinically diagnosed tooth sensitivity at screening.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02773758
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 4
Start date January 1, 2016
Completion date March 11, 2016

See also
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