drugset / Trial / NCT07352956

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

NCT07352956

Completed 177 enrolled HALEON
RandomizedParallel-groupSingle-blindTreatment

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.

Timeline

Start
2026-01-16
Primary completion
2026-04-06
Completion
2026-04-06

Drugs

EvaluationDrugModalityDoseRoute
Subject sodium fluoride Unknown Oral
Subject stannous fluoride Small molecule 0.454 % Oral

Indications