At a glance
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Clinical Evaluation of Clinpro™ 2.1% Sodium Fluoride Aqueous Solution in the Treatment of Dentin Hypersensitivity
In Brief
A clinical study evaluating 3M™ Clinpro™ Fluoride Aqueous Solution and 3M™ Vanish™ for Dentin Hypersensitivity. Completed, enrolled 101 participants across 1 site.
Detailed Summary
The goal of this clinical trial is to evaluate the effect of 3M™ Clinpro™ Fluoride Aqueous Solution (experimental) on Dentin Hypersensitivity (DHS) in comparison to 3M™ Vanish™ (commercialized, control\] in patients who have DHS. Participants will be asked to complete the following activities: Undergo a pre-treatment washout period for 3- to 6-weeks (± 4 days) post-enrollment. During this time, the Subject is to only use the provided oral hygiene products. Hypersensitivity will be assessed prior to (baseline) and immediately after sample application. Subject will be asked to come to the facility for hypersensitivity assessments at 24 hours, 7 days, and 30 days after the treatment visit. Researchers will compare 3M™ Clinpro™ Fluoride Aqueous Solution to 3M™ Vanish™ to evaluate if the effect of Clinpro™ on DHS treatment is non-inferior to Vanish™.
Study Details
Timeline
Interventions
Hypersensitivity treatment. Apply once after baseline measurement of dentin sensitivity.
Hypersensitivity treatment. Apply once after baseline measurement of dentin sensitivity.