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COMPLETED
NCT07741032
NA

A Study to Evaluate the Dentinal Hypersensitivity Efficacy of Two Experimental Mouthwash Formulations

Sponsor: HALEON

View on ClinicalTrials.gov

Summary

The aim of this study is to evaluate the clinical efficacy of two experimental mouthwash formulations, against a placebo mouthwash (without experimental ingredients). One experimental formulation to be used either once daily or twice daily, and the second experimental formulation and placebo, to be used twice daily for the treatment of dentinal hypersensitivity.

Official title: A Proof of Concept Study to Evaluate the Efficacy of Two Experimental Mouthwash Formulations in the Relief of Dentinal Hypersensitivity

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

118

Start Date

2012-03-26

Completion Date

2012-07-09

Last Updated

2026-08-03

Healthy Volunteers

No

Interventions

OTHER

3% KNO3 Mouthwash

3.0% weight by weight (w/w) KNO3 with 217 parts per million (ppm) sodium fluoride.

OTHER

2% HPC Mouthwash

2.0% w/w HPC mouthwash with 217ppm sodium fluoride.

OTHER

0% KNO3 Mouthwash

0% w/w KNO3 with 217ppm sodium fluoride.

Locations (1)

proDERM

Harburg, Free and Hanseatic City of Hamburg, Germany