Effects of an Oxalate Containing Product on Dentinal Hypersensitivity With Dental Prophylaxis

Completed · Not applicable

Conditions studied: Dentin Sensitivity

In brief

This study will assess sensitivity during a dental prophylaxis with or without the use of a potassium oxalate salt solution.

Key facts

Study ID

NCT02481557

Run by

Procter and Gamble

People needed

36

Starts

2015-06-01

Expected to finish

2015-06-01

Last updated by the study team

2019-06-11

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 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.

You may not qualify if…

• 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
• inability to undergo study procedures
• fixed orthodontic appliances

Where it is running

• Silverstone Research Group — Las Vegas, Nevada, United States

Full record on ClinicalTrials.gov

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