Trial Condition(s):
A study to evaluate cooling sensation of an allergy product in adults with a history of allergies
21048
Not Available
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In this study, researchers are primarily interested in evaluating the level of agreement of cooling sensation provided by this chewable, flavored, allergy medicine. Participants joining this study will receive one test drug tablet and be asked to chew completely before swallowing the drug. A questionnaire will be used to collect the feedback from participants. The study will involve only one (1) visit and participant will stay in this study for about 60-75 minutes to evaluate the cooling sensation as well as other sensory attributes perceived in the mouth, nose and throat.
- Female or male adults aged 18 to 65 years of age inclusive - Be in good general health - Previous self-reported sufferers of upper respiratory allergies who at the time of the study are either asymptomatic, symptomatic but not treating and agree to use study medication or symptomatic and treating with an allergy medicine that is not an antihistamine - Agree to not use antihistamine products 24 hours before and after the treatment - Willing to avoid eating food or candy (other than crackers consumed during testing), drinking any liquid other than water, gum chewing and teeth brushing one hour prior to testing
- Individuals who have used oral/systemic medications 24 hours before the first administration of test product - Individuals who use medications which may influence taste perception - Individuals who have received or used an investigational new drug in the last 30 days or have been an active participant in another clinical or market research study in the last 30 days - Women who are pregnant or thinking of becoming pregnant or are nursing - Participants with congestion at the time of study visit - Any self-reported symptoms or conditions that may interfere with the participants ability to complete the evaluation of the product on testing day - Any current medical condition that in the opinion of the Investigator or designee may interfere with normal taste and/or temperature perception (e.g., active common cold, sinus infection, bronchial infection, adenoids, paresthesia etc.) - History of alcohol or drug abuse - History of hypersensitivity or allergic reactions to any ingredients in the test product - Individuals with a history of glaucoma, liver or kidney disease, respiratory conditions such as chronic bronchitis or swallowing difficulties - Individuals who are currently wearing any kind of dental braces or with dental work or have cavities and associated pain that may affect their ability to chew a tablet
Locations | Status | |
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Locations Investigative Site Teaneck, United States, 07666 | Status Completed | Contact Us: E-mail: [email protected] Phone: (+)1-888-84 22937 |
An open label, multi-center study to evaluate sensory attributes of an antihistamine product
Trial Type:
Interventional
Intervention Type:
Drug
Trial Purpose:
Other
Allocation:
N/A
Blinding:
N/A
Assignment:
Single Group Assignment
Trial Arms:
1
Not Available