Research on Oral Tolerability and Product Application/Response of Two Oxalate Products for Dental Patients With Risk of Dentinal Hypersensitivity

• Status: Completed
• Trial end date: 2016-06-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will assess the oral tolerability and immediate post-treatment safety of topical application for two marketed oxalate products as initial care in dental patients to treat or prevent tooth sensitivity pain that may be attributed to dentinal hypersensitivity.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Procter and Gamble
• Treatments: Fluorides; Tin Fluorides

Criteria

Inclusion Criteria:

• be at least 18 years of age

• sign an informed consent form and be given a copy

• be in good general health as determined by the Investigator/designee

• agree to not participate in any other oral care study for the duration of this study

• agree to return for scheduled visits and follow all study procedures

• have at least one tooth at risk for hypersensitivity.

Exclusion Criteria:

• any medical condition requiring pre-medication prior to dental procedures

• any diseases or conditions that might interfere with the subject safely completing the study

• inability to undergo study procedures

• a history of kidney stones

• have self-reported pregnancy or nursing

• known allergies to the following ingredients; aqua, glycerin, cellulose gum, dipotassium oxalate, carbomer, sodium hydroxide, sodium benzoate, or potassium sorbate