The Effect of Biotene® on the Symptoms of Xerostomia and Mastication and Swallowing
Xerostomia, Hyposalivation
About this trial
This is an interventional supportive care trial for Xerostomia focused on measuring swallowing, saliva, oral health, mastication, quality of life, artificial saliva
Eligibility Criteria
Inclusion Criteria:
- Medically stable adults
- Age 19 years of age or older
- Able to sit upright independently and transfer to a chair
- Able to eat foods requiring mastication
- Decision-making capacity to provide informed consent
Exclusion Criteria:
- Acute illness or uncontrolled medical condition
- Allergies to any pharmaceuticals
- Allergies to medical tape/adhesive
- Allergies to Nabisco Saltines® or any of the ingredients
- Participant-reported issues with excess saliva and/or drooling
- Open ulcerations in the oral cavity.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Biotene® followed by Sham
Sham followed by Biotene®
Recruited volunteers will each participate in two experimental sessions. Participants will be randomized into either Protocol A or Protocol B. In their first session, participants in Protocol A will undergo baseline mastication, swallowing, salivary, and oral health-related quality of life testing, then they will receive the experimental condition. For the experimental condition, participants will be instructed to apply Biotene® Oralbalance Moisturizing Gel according to package directions. Testing will then be repeated. In the second session, after baseline testing, participants will receive the sham condition (instead of the experimental condition). For the sham condition, participants will be instructed to rinse their mouth with room temperature distilled water. Testing will then be repeated.
Recruited volunteers will each participate in two experimental sessions. Participants will be randomized into two protocols: 1) Protocol A and 2) Protocol B. In their first session, participants in Protocol B will undergo baseline mastication, swallowing, salivary, and oral health-related quality of life testing, then they will receive the sham condition. Testing will then be repeated. In the second session, after baseline testing, participants will receive the experimental condition (instead of the sham condition). Testing will then be repeated.