Research on Oral Tolerability and Product Application/Response of Two Oxalate Products for Dental Patients With Risk of Dentinal Hypersensitivity
| Status: | Completed |
|---|---|
| Conditions: | Neurology |
| Therapuetic Areas: | Neurology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 7/21/2016 |
| Start Date: | November 2015 |
| End Date: | June 2016 |
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.
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.
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
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