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COMPLETED
NCT07738198
PHASE3

Dentin Hypersensitivity Reduction Efficacy Clinical

Sponsor: Colgate Palmolive

View on ClinicalTrials.gov

Summary

The objective of this study is to assess clinical efficacy of a toothpaste containing stannous fluoride (Colgate-Palmolive Company, New York, NY, USA) to provide dental hypersensitivity relief (tactile and air blast) in comparison to commercially available potassium-based desensitizing toothpaste (Senodyne Extra Whitening Toothpaste, GasoSmithKline Co., UK) and commercially available non-desensitizing toothpaste (Colgate Cavity Protection Toothpaste, Colgate-Palmolive Company, New York, NY, USA) over a seven day study period

Official title: Dentin Hypersensitivity Reduction Efficacy of a Dentifrice Containing Stannous Fluoride as Compared to Commercially-available Potassium-based Desensitizing Toothpaste.

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

116

Start Date

2018-11-26

Completion Date

2018-12-08

Last Updated

2026-07-31

Healthy Volunteers

Yes

Interventions

DRUG

0.454% stannous fluoride toothpaste

brush twice daily (morning and evening) Duration of exposure: one (1) minute

DRUG

5% potassium nitrate

Brush twice daily (morning and evening) Duration of exposure: one (1) minute

DRUG

0.76% sodium monofluorophosphate

Brush twice daily (morning and evening) Duration of exposure: one (1) minute

Locations (1)

FAR Oral and Systemic Health Consulting, Inc

Costa Mesa, California, United States