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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.
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Inclusion criteria
No clinically significant and relevant abnormalities in medical history or upon oral examination.
Absence of any condition that would impact on the participant's safety or wellbeing or affect the individual's ability to understand and follow study procedures and requirements.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
221 participants in 3 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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