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A Study to Evaluate the Dentinal Hypersensitivity Efficacy of Two Experimental Mouthwash Formulations
Sponsor: HALEON
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
Conditions
Interventions
3% KNO3 Mouthwash
3.0% weight by weight (w/w) KNO3 with 217 parts per million (ppm) sodium fluoride.
2% HPC Mouthwash
2.0% w/w HPC mouthwash with 217ppm sodium fluoride.
0% KNO3 Mouthwash
0% w/w KNO3 with 217ppm sodium fluoride.
Locations (1)
proDERM
Harburg, Free and Hanseatic City of Hamburg, Germany