Clinical Trial

A Clinical Study to Evaluate the Effectiveness of an Test Toothpaste for the Relief of Dentin Hypersensitivity in a Chinese Population

Completed
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Summary
The purpose of this study is to evaluate the clinical efficacy of a 0.454 percent (%) weight/weight (w/w) stannous fluoride (SnF2) toothpaste in reducing dentin hypersensitivity (DH) to an evaporative (air) stimulus and tactile stimulus after 28 and 56 days twice daily brushing.
Protocol Amendment History 2 changes
critical Trial completed 2026-04-15
notable Enrollment increased: 100 -> 177 participants 2026-04-15
Trial Details
NCT Number NCT07352956
Lead Sponsor HALEON
Conditions Dentin Sensitivity
Enrollment 177 participants
Start Date 2026-01-16
Primary Completion 2026-04-06 (estimated)
Study Completion 2026-04-06 (estimated)
Updated on ClinicalTrials.gov 2026-04-14