drugset / Trial / NCT03965039

A Clinical Study to Assess the Effects of Various Dentifrice Technologies on Dentinal Hypersensitivity

NCT03965039

Completed 120 enrolled Procter and Gamble
RandomizedParallel-groupTriple-blindTreatment

Summary

The objective of this study is to evaluate the efficacy (changes in dentinal hypersensitivity) and safety (oral soft tissue evaluation) after use of one of four dentifrices in subjects with pre-existing hypersensitivity over an 11-week period.

Timeline

Start
2019-07-08
Primary completion
2019-10-03
Completion
2019-10-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Potassium Nitrate Other / unclassified 5 % Topical
Comparator stannous fluoride Small molecule 0.454 % Topical
Comparator sodium monofluorophosphate Unknown 0.76 % Topical

Indications