A Study to Investigate a Method to Measure Food Occlusion by Denture Adhesives in Denture Wearers

Exclusion Criteria

• •An investigational site staff member directly involved in the conduct of the study or their family member, site staff members otherwise supervised by the investigator, or an employee of the sponsor directly involved in the conduct of the study.
• •Participation in any other clinical study involving investigational drugs, cosmetics or medical devices within 30 days prior to study entry and/or during study participation.
• •Acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.
• •Pregnant female participants.
• •Breastfeeding female participants.
• •Known or suspected intolerance or hypersensitivity to the study materials (or closely related compounds) or any of their stated ingredients.
• •Unwilling or unable to comply with the Lifestyle Guidelines described in this protocol.
• •History of swallowing difficulties or choking.
• •Currently taking or have taken a bisphosphonate drug (i.e., Fosamax®, Actonel®, Boniva®) for treatment of osteoporosis.
• •Any clinically significant or relevant oral abnormality (e.g. temporomandibular joint \[TMJ\] problems) that, in the opinion of the investigator, could affect the participants participation in the study.
• •Known allergy to peanuts or any other nut.
• •Any condition or medication which, in the opinion of the investigator, is currently causing xerostomia.
• •Recent history (within the last year) of alcohol or other substance abuse.
• •OST examination findings such as stomatitis, open sores, lesions, redness or swelling which in the opinion of the investigator, would interfere with the conduct of the study.
• •Use of any medication that, in the opinion of the investigator, would interfere with the conduct of the study.
• •A serious chronic disease requiring intermittent hospital visits.
• •Having been previously enrolled in this study.
• •Any participant who, in the opinion of the investigator, should not participate in the study.