Collection of Clinical Data and Specimens for Research in Hearing, Balance, Taste, Smell, Voice, Speech, and Language Disorders.
概览
- 阶段
- 不适用
- 干预措施
- Patients
- 疾病 / 适应症
- Hearing Loss
- 发起方
- National Institute on Deafness and Other Communication Disorders (NIDCD)
- 入组人数
- 600
- 试验地点
- 1
- 主要终点
- Clinical data collection
- 状态
- 招募中
- 最后更新
- 4天前
概览
简要总结
Background:
People with hearing, balance, and taste, smell, voice, speech, language, and other Ear, Nose, and Throat (ENT) disorders may seek treatment at the National Institute on Deafness and Other Communication Disorders (NIDCD). Some of these people may benefit from enrolling in the NIDCD intramural research program to receive their care. Enrolling will also allow investigators to collect participants clinical data and specimens for future research.
Objective:
This natural history study has 2 goals: (1) to collect data and specimens that may be used for research; and (2) to evaluate participants who may be candidates for other research studies.
Eligibility:
People aged 2 years or older with a hearing, balance, and communication disorder. Those at risk or who are suspected of having such a disorder are also eligible.
Design:
Participants will be screened. Their medical records will be reviewed.
Participants will agree to have their medical data used for research. Specimens such as blood or other tissue samples may also be used for research. All data and specimens will be collected during their routine care visits.
All tests done will be the normal care for each participant s condition. No tests will be done solely for research.
Some of these tests may require blood or tissue samples. Some may use special tools to test hearing and balance. Some may test heart or lung function. These tests may also include different types of imaging scans.
All tests will be explained. Participants may ask questions at any time.
Participants may remain in this study for up to 2 years. If they need further care, they may sign a new consent.
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详细描述
Study Description: It may be in the interest of the NIDCD Clinical Research Program (CRP) to collect clinical data or specimens generated in the diagnosis and treatment of hearing, balance, taste, smell, voice, speech, language, and other Ear, Nose, and Throat (ENT) disorders and to evaluate patients to determine candidacy for intramural clinical studies. This protocol will provide the administrative vehicle to enable the evaluation and provision of clinical care for patients with hearing, balance and communication disorders by the NIDCD CRP, Clinical Center, and consult services as well as to provide a repository of information on enrolled subjects to allow for hypothesis generation in future research. No investigational therapies will be administered in this study. As part of hypothesisgenerating research related to taste and oral sensation, participants may undergo brief sensory testing using food-grade tannic acid solutions. This testing is designed to characterize taste, mouthfeel, and chemesthetic responses and does not involve administration of investigational agents or swallowing of test solutions. Objectives: * To provide a repository of data and samples collected from clinical data or specimens generated in the diagnosis and treatment of hearing, balance, taste, smell, voice, speech, language, and other ENT disorders to allow for hypothesis generation in future research. * To evaluate patients to determine candidacy for intramural clinical studies
研究者
入排标准
入选标准
- •INCLUSION CRITERIA:
- •In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- •Patients must be age 2 years or older if procedures or treatment are required.
- •Patients at risk, suspected of having, have a history of, or currently have a diagnosed hearing, balance, taste, smell, voice, speech, language, and other ENT disorder.
- •An NIDCD clinical investigator and PI determines it is in the interest of the patient/individual and NIDCD CRP for the subject to undergo consult, treatment or follow-up at the NIDCD/NIH
- •Patient or their Legally Authorized Representative is able to provide informed consent. The consent form will be signed by parents or guardians of patients under the age of
- •A subset of enrolled participants with known or suspected PIEZO2-related sensory dysfunction may be asked to participate in the remote taste and oral somatosensory testing procedures. Participation in this component is optional and not required for enrollment or continued participation in the parent protocol.
排除标准
- •An individual who meets any of the following criteria will be excluded from participation in this study:
- •Candidates who do not meet the inclusion criteria.
- •Candidates who in the opinion of the PI and clinical team have medical or unstable conditions for which NIDCD and CC consultative services are unable to provide or support optimal care
- •Participants without known or suspected PIEZO2-related sensory dysfunction will not be asked to complete the sensory testing component. Additional exclusion criteria for taste testing only procedures include:
- •Active oral sores, open cuts, or significant oral pain
- •Recent oral surgery or dental procedures within the past 7 days
- •Known allergy or hypersensitivity to tannins or polyphenols
- •Acute upper respiratory infection or conditions that may interfere with taste perception
研究组 & 干预措施
Patients
Patients at risk, suspected of having, have a history of, or currently have a diagnosed hearing, balance or communication disorder.
结局指标
主要结局
Clinical data collection
时间窗: Ongoing
To collect clinical data or specimens generated in the diagnosis and treatment of hearing, balance and communication disorders
Evaluation for clinical studies
时间窗: Ongoing
To evaluate patients to determine candidacy for intramural clinical studies