HALEON
The aim of this clinical study is to evaluate the efficacy of an experimental mouthwash used with a marketed whitening toothpaste or a marketed regular fluoride toothpaste, compared to a marketed regular fluoride toothpaste alone, in preventing extrinsic dental stain build-up.
This will be a single-center, 12-week, randomized, controlled, examiner-blind, 3 treatment-arm, parallel-group, stratified clinical study in healthy participants to evaluate impact on the build-up of dental stain after 12 weeks twice daily use of an experimental mouthwash with either a marketed whitening toothpaste containing 5 percent (%) potassium nitrate (KNO3) and 0.25% sodium fluoride (NaF) or with a marketed regular fluoride toothpaste containing 0.25% NaF compared with use of a marketed regular fluoride toothpaste containing 0.25% NaF. Sufficient participants will be screened to ensure…
Inclusion Criteria: * Participant provision of a signed and dated informed consent document indicating that the participant has been informed of all pertinent aspects of the study before any assessment is performed. * Participant is willing and able to comply with scheduled visits, treatment/application/dosing plan, study restrictions, lifestyle considerations and other study procedures. * A participant in good general and mental health with, in the opinion of the investigator or medically qualified designee, no clinically significant or relevant abnormalities in medical history or upon oral…
A toothpaste containing 5% KNO3 and 0.25% NaF.
A mouthwash containing Dipotassium Oxalate.
A marketed regular fluoride toothpaste containing 0.25% NaF.
Arctuva estimate
Verify or correct the compensation shown for this listing.