This study is currently recruiting participants.
Number
001560-DC
Sponsoring Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Recruitment Detail
Type: Participants currently recruited/enrolled Gender: Male & Female Min Age: 3 Years Max Age: 99 Years
Referral Letter Required
No
Population Exclusion(s)
None
Keywords
Hearing; Balance; Speech; Taste; SMELL; Tissue Sample; Genomic DNA; Saliva
Recruitment Keyword(s)
Condition(s)
Hearing Loss; Head and Neck Neoplasms; hearing disorders; Laryngeal Disease
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Supporting Site
National Institute on Deafness and Other Communication Disorders
Many disorders of the head and neck can affect a person s hearing; balance; smell; taste; swallowing; voice; or speech. These disorders include cancers and genetic and inflammatory diseases. To find better ways to diagnose and treat these disorders, researchers need to study tissues and other biological samples from people who have them.
Objective:
To collect biological samples for a repository that will be used for research.
Eligibility:
People of any age with a disorder of the head and neck that requires the taking of biological samples. The conditions may be any that affect hearing; balance; smell; taste; swallowing; voice; or speech.
Design:
Part 1: Participants will give permission for their leftover tissue samples to be used for research. These are tissue samples from the head and neck that were collected in the course of routine tests and care or other research studies. Information on each participant s age, diagnosis, and previous treatments will also be collected.
Part 2: Some participants may be asked for more samples. All those aged 3 years or older will have a physical exam. They will provide blood and saliva samples. A cotton swab or brush will be used to collect cells from the inside of the cheek.
Participants 18 years or older may have additional tests. They may provide nasal secretions: A piece of gelfoam or a sponge will be placed in the nose to soak up secretions for 5 to 10 minutes. They may have biopsies: Small samples of tissue will be cut from the skin and the tissue lining the mouth.
Samples may be used for genetic testing.
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INCLUSION CRITERIA In order to be eligible to participate in this study, an individual must meet all of the following criteria: - Ability to provide their own consent, or for minors, a parent or guardian is able to consent on their behalf. - Ability of subject (or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document. - Have a hearing, balance, smell, taste, voice, speech or language condition for which the subject is under clinical care or research purposes under a separate Review Board (IRB) approved protocol; OR be a healthy volunteer aged at least 3 years, enrolled on an approved research protocol. EXCLUSION CRITERIA An individual who meets any of the following criteria will be excluded from participation in this study: - Have active symptomatic major organ disorders that would increase the risk of biopsy for research, including but not limited to bleeding disorders, ischemic heart disease, a recent myocardial infarction, active congestive heart failure or severe pulmonary dysfunction - Have specific medical condition, such as a bleeding tendency where additional biopsies or phlebotomy procedures may increase the subjects risk in participating. This will be determined at the discretion of the principal investigator.
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- Ability to provide their own consent, or for minors, a parent or guardian is able to consent on their behalf.
- Ability of subject (or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.
- Have a hearing, balance, smell, taste, voice, speech or language condition for which the subject is under clinical care or research purposes under a separate Review Board (IRB) approved protocol; OR be a healthy volunteer aged at least 3 years, enrolled on an approved research protocol.
EXCLUSION CRITERIA
An individual who meets any of the following criteria will be excluded from participation in this study:
- Have active symptomatic major organ disorders that would increase the risk of biopsy for research, including but not limited to bleeding disorders, ischemic heart disease, a recent myocardial infarction, active congestive heart failure or severe pulmonary dysfunction
- Have specific medical condition, such as a bleeding tendency where additional biopsies or phlebotomy procedures may increase the subjects risk in participating. This will be determined at the discretion of the principal investigator.
Principal Investigator
Referral Contact
For more information: