Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis | NCT02481557 | Trialant
CompletedInterventionalNot ApplicableUpdated Jun 11, 2019
Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis
ClinicalTrials.gov ID
NCT02481557
Lead Sponsor
Procter and GambleINDUSTRY
Overall Status
Completed
Study Type
Interventional
Phase
Not Applicable
Enrollment
36Actual
Last Update Posted
Jun 11, 2019Actual
Start Date
Jun 2015
Primary Completion Date
Jun 2015Actual
Completion Date
Jun 2015Actual
Brief Summary
This study will assess sensitivity during a dental prophylaxis with or without the use of a potassium oxalate salt solution.
Dentin Sensitivity
Oxalate Salt Solution
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
Yes
Eligibility 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 delay any elective dentistry, and to report any dentistry received during the course of the study
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 with a Schiff sensitivity score of at least 1 in response to air challenge and a Yeaple Probe score of 10-40 in response to tactile challenge.
Exclusion Criteria:
severe periodontal disease, as characterized by purulent exudate, generalized mobility, and/or severe recession
active treatment for periodontitis
any diseases or conditions that might interfere with the subject safely completing the study