- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00220038
Experiments to Test How and Why the Sense of Smell Differs Between People
January 10, 2012 updated by: Rockefeller University
Genetic Basis of Specific Anosmias
The ability to smell varies greatly between different individuals.
Some people are unable to detect an odor that most people can smell.
It is not known what causes these individual differences.
Humans have about 1000 genes for odorant receptors that bind and detect odor molecules.
It has been shown that some of these genes exist in two forms: a functional one and one that has been mutated and is therefore no longer functional.
We think that people who can not smell a specific odor may carry the non-functional form of the gene for the receptor that detects the odor molecule.
To test this hypothesis we want to find people who can not detect a specific smell and then compare their odorant receptor genes with those of people who can smell the odor.
Study Overview
Detailed Description
The enjoyment of a fine wine, the odor of a ripe cheese, the memory of a long-lost grandmother brought back by the scent of her perfume, or the alarm we feel when we smell smoke are all produced by a functioning olfactory system.
Interestingly, there are enormous individual differences in how we interpret these smells.
Given almost any odor, some people will find it pleasant, others unpleasant.
Ripe cheese or garlic may smell delicious to some, but repulsive to others.
The scientific basis of this variation has not been well-studied.
Despite the clear evidence for culture-based preferences for food and aromas, the nature-versus-nurture debate for smell remains unresolved.
We believe there may be a genetic basis for our unique senses of smell.
For example, some of us can smell methanethiol, the metabolite that is excreted in our urine after eating asparagus, whereas other people cannot.
The Rockefeller University Smell Study seeks to recruit 400 normal subjects to track down the genetic basis of how we perceive smells.
The study consists of up to two visits, each lasting up to 4 hours, in which we will test your perception of a variety of smells.
On your first visit there will be a small blood sample taken (8.5 millileters) and your height and weight will be measured.
If you are a woman of child-bearing age, we will ask you to provide a urine sample to test for pregnancy.
If you are pregnant, you will not be permitted to participate in our study.
You will fill out a short survey that asks some questions about yourself, your household, your personal habits, and your sense of smell.
You will perform three different types of smell tests.
In the first, you will be given two vials at a time and asked to tell us which contains an odor.
In the second type of test, you will be asked to describe carefully your impression of three different odors.
In the third type of test, you will be asked to rate odors according to their strength and pleasantness.
All odorants will be presented to you in glass jars.
You will be asked to smell odors in several hundred jars.
Study Type
Observational
Enrollment (Actual)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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New York
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New York, New York, United States, 10021
- Rockefeller University Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
700 healthy normal volunteers will be recruited from the New York City area
Description
Inclusion Criteria:
18 years or older,
Male and Female
Normal sense of smell
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Exclusion Criteria:
Not pregnant
No history of nasal illness or surgery
No seasonal allergies-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Normal
700 healthy adult volunteers will be drawn from the New York City area
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subjects are instructed to sniff two vials, one containing the solvent, the other a dilution of the odorant.
They are asked to scan the vial with the stronger odor.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Leslie B. Vosshall, PHD, Rockefeller University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2004
Primary Completion (Actual)
January 1, 2007
Study Completion (Actual)
May 1, 2010
Study Registration Dates
First Submitted
September 21, 2005
First Submitted That Met QC Criteria
September 21, 2005
First Posted (Estimate)
September 22, 2005
Study Record Updates
Last Update Posted (Estimate)
January 11, 2012
Last Update Submitted That Met QC Criteria
January 10, 2012
Last Verified
January 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LVO-0539
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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