drugset / Trial / NCT06378008

A Clinical Study to Evaluate the Anti-Sensitivity Effect of a Calcium Sodium Phosphosilicate Toothpaste in a Population of Dentin Hypersensitivity Sufferers

NCT06378008

Completed 217 enrolled HALEON
RandomizedParallel-groupSingle-blindTreatment

Summary

The aim of this study is to confirm the clinical dentin hypersensitivity (DH) efficacy of a 5 percent (%) calcium sodium phosphosilicate (CSPS) toothpaste.

Timeline

Start
2024-04-16
Primary completion
2024-09-04
Completion
2024-09-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fluoride Other / unclassified 1100 ppm Topical
Subject PHOSPHINE SILANE Other / unclassified 5 % Topical

Indications