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

Completed · Not applicable

Conditions studied: Dentinal Hypersensitivity

In brief

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.

Key facts

Study ID

NCT02613117

Run by

Procter and Gamble

People needed

104

Starts

2015-11-01

Expected to finish

2016-06-01

Last updated by the study team

2020-09-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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

Where it is running

• Tufts University School of Dental Medicine — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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