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

Completed · Not applicable

Conditions studied: Dentin Sensitivity

In brief

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.

Key facts

Study ID

NCT02513212

Run by

Procter and Gamble

People needed

24

Starts

2015-07-01

Expected to finish

2015-09-01

Last updated by the study team

2020-08-31

Who can join

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

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• Chad J Anderson DMD Inc — Fresno, California, United States

Full record on ClinicalTrials.gov

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