NCT01039935CompletedNot Applicable
Genetic Basis of Odor Discrimination
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Rockefeller University
- Enrollment
- 512
- Locations
- 1
- Primary Endpoint
- Percentage of correct responses when discriminating between (-)-carvone and (+)-carvone, isovaleric acid and isobutyric acid, androstenone and androstadienone DNA sequence of ORs sensitive to these odors
Study Overview
Brief Summary
Prior to the main study we will perform a pilot study on 60 subjects. The purpose of the pilot study is to identify the range of odor concentrations that will be used in the main study and to optimize the tasks performed in the main study.
Study Design
- Study Type
- Observational
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to 50 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Current non-smokers
Exclusion Criteria
- •Current smokers
- •Allergy to fragrances or smells of any kind
- •Active head cold, upper respiratory infection, or seasonal nasal allergies
- •History of nasal health problems, including endoscopic nasal surgery for sinus conditions or polyp removal.
- •Pre-existing medical condition that has caused anosmia or near total loss of the sense of smell, such as: head injury, cancer therapy, radiation to head and neck, or alcoholism
Outcomes
Primary Outcomes
Percentage of correct responses when discriminating between (-)-carvone and (+)-carvone, isovaleric acid and isobutyric acid, androstenone and androstadienone DNA sequence of ORs sensitive to these odors
Time Frame: 3 years
Secondary Outcomes
- concentration at which odors need to be added to allow for discrimination; thresholds to all six odors; verbal descriptors assigned to all six odors(3 years)
Investigators
Study Sites (1)
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