Clinical Study to Investigate the Ability of a Stannous Fluoride Toothpaste to Protect From Dentine Hypersensitivity

Exclusion Criteria

• •Participant is an employee of the investigator site directly involved in the conduct of the study, or an employee of the investigator site otherwise supervised by the investigator, or a member of their immediate family.
• •Participant is an employee of the sponsor directly involved in the conduct of the study or a member of their immediate family.
• •Female participant who is pregnant or intending to become pregnant during the study (self-reported).
• •Female participant who is breastfeeding (self-reported).
• •Participant with known or suspected intolerance or hypersensitivity to the study products, any of their stated ingredients or closely related compounds (self-reported).
• •Participant with a recent history (within the last year) of alcohol or other substance abuse (self-reported).
• •Participant is participating in or has participated in other studies (including non-medicinal studies) involving investigational product(s) within 30 days of Screening (Visit 1) or plans to participate in other studies (including non-medicinal studies) during this study.
• •Participant has participated in a tooth sensitivity study within 8 weeks of Screening (Visit 1).
• •Participant is currently using an oral care product indicated for DH relief or care of sensitive teeth or has used such a product within 8 weeks of Screening (Visit 1).
• •Participant takes daily doses of medications/treatments which, in the opinion of the investigator or medically qualified designee, could interfere with their perception of tooth sensitivity (for example, analgesics, anticonvulsants, antihistamines that cause marked or moderate sedation, sedatives, tranquilizers, antidepressants, mood-altering and anti-inflammatory drugs).
• •Screening (Visit 1): Participant has taken antibiotics in the 2 weeks prior to Screening (Visit 1).
• •Baseline (Visit 2): Participant has taken antibiotics in the 2 weeks prior to Baseline (Visit 2), that is, during the acclimatization period.
• •Participant takes daily doses of a medication which, in the opinion of the investigator or medically qualified designee, is causing xerostomia.
• •Participant requires antibiotic prophylaxis for dental procedures.
• •Participant has had professional tooth de-sensitizing treatment within 8 weeks of Screening (Visit 1).
• •Participant has had a tooth bleaching procedure within 8 weeks of Screening (Visit 1).
• •Participant has had dental prophylaxis within 4 weeks of Screening (Visit 1).
• •Participant has had treatment for periodontal disease (including surgery) within 12 months of Screening (Visit 1).
• •Participant has had scaling or root planning within 3 months of Screening (Visit 1).
• •Participant with gross periodontal disease.
• •Participant with a tongue or lip piercing.
• •Participant with evidence of gross intra-oral neglect or the need for extensive dental therapy.
• •Participant with a fixed or removable partial prosthesis which, in the opinion of the investigator or dentally qualified designee, could impact study outcomes.
• •Participant with multiple dental implants which, in the opinion of the investigator or dentally qualified designee, could impact study outcomes.
• •Participant has had orthodontic treatment (fixed or removable orthodontic braces/bands) within 6 months of Screening (Visit 1).
• •Participant with a fixed or removable orthodontic retainer which, in the opinion of the investigator or dentally qualified designee, could impact study outcomes (for example, participant who is an intermittent user of a removable orthodontic retainer). Note: Teeth involved in a fixed orthodontic retainer may be used as 'test teeth' if, in the opinion of the investigator or dentally qualified designee, their selection would not impact study outcomes.
• •Specific Dentition Exclusions for 'Test teeth':
• •1. Tooth with evidence of current/recent dental caries.
• •2. Tooth having had (self-reported) treatment for dental caries within 12 months of Screening (Visit 1).
• •3. Tooth with exposed dentine and deep, defective, or facial restorations.
• •4. Tooth with a full crown or veneer.
• •5. Tooth adjacent to a bridge abutment or crown which, in the opinion of the investigator or dentally qualified designee, could impact study outcomes.
• •6. Sensitive tooth with contributing etiologies other than EAR to exposed dentine.
• •7. Sensitive tooth not expected to benefit from use of a sensitivity toothpaste, in the opinion of the investigator or dentally qualified designee.
• •Participants who, in the opinion of the investigator or designee, are unable to provide appropriate responses to the Labelled Magnitude Scale (LMS) training questions.
• •Participants who, in the opinion of the investigator or medically qualified designee, should not participate in the study.