A Clinical Study to Determine the Safety and Effectiveness of Dentinal Hypersensitivity Treatment With Two Different Toothbrushes

• Status: Completed
• Trial end date: 2015-09-01
• Target enrollment: 0
• Participant gender: All

Summary

This study will determine the effects toothbrush type (power or manual) has on the safety and effectiveness of professional dentinal hypersensitivity treatment with a marketed oxalate-containing solution.

• 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;

• provide written informed consent prior to participation and be given a signed copy of the informed consent form;

• complete a photography consent agreement pertaining to the collection and use of non-identifying intraoral photographs;

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

• have at least one tooth with a Schiff sensitivity score of at least 1 in response to the cool air challenge.

Exclusion Criteria:

• self-reported pregnancy or nursing;

• severe periodontal disease, as characterized by purulent exudate, generalized mobility, and/or severe recession;

• active treatment of periodontitis;

• any diseases or conditions that might interfere with the safe completion of the study; or

• an inability to undergo any study procedures.