drugset / Trial / NCT06010732

In Situ Comparison of the Remineralization Potential of Optimized Fluoride Dentifrice With Control Fluoride Dentifrice

NCT06010732 ↗

Phase 3 Completed 52 enrolled Indiana University HALEON · collab
RandomizedCrossoverTriple-blindPrevention

Summary

The purpose of this study is to compare the remineralization potential of an optimized fluoride dentifrice to a control fluoride dentifrice in an in situ caries model.

Timeline

Start
2023-10-02
Primary completion
2024-02-22
Completion
2024-02-22

Outcome

Missed primary endpoint

registry analysis (superiority test); 1100 Ppm F as Sodium Fluoride (Positive Control) vs 1100 Ppm F as Sodium Fluoride Test Product; p = 0.986; NCT06010732 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject sodium fluoride Unknown 1100 ppm —

Indications