Risk Factors and Potential Causes of Eustachian Tube Dysfunction in Adults
NCT ID: NCT01251432
Last Updated: 2016-11-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
30 participants
OBSERVATIONAL
2010-06-30
2016-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In this study, the investigators plan to explore the relationship between the results of the standard Eustachian tube function tests and those for the anatomy and function of the Eustachian tube in adults with a disease condition likely to be caused by poor Eustachian tube function. Also, there are a number other disease conditions (examples: nasal allergy, acid reflux disease) that are related to poor Eustachian tube function and it is possible that these conditions and their effect on Eustachian tube function can be treated with medicines. Therefore, the investigators also plan to evaluate enrolled persons for those conditions. It is expected that if the results of the standard Eustachian tube function tests can be explained by the anatomy of the back of the nose and Eustachian tube, the functional anatomy (movements during swallowing etc) of the Eustachian tube or the presence of allergy and or/acid reflux disease, new medical and/or surgical treatments can be developed to improve Eustachian tube function and "cure" or treat the associated middle-ear diseases.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
If the subject is eligible and signs informed consent to participate in the study, a series of questions regarding past history of ear disease will be asked as well as whether or not a subject has any of several risk factors that makes people more likely to develop otitis media with effusion and other ear diseases. The subject will also complete a short questionnaire that asks questions about whether or not they have symptoms consistent with acid reflux disease. Then, a blood sample (about 2/3 of a tablespoon) will be taken from an arm vein and sent to a laboratory for assay of chemicals associated with allergic diseases. These procedures should take about 30 minutes to complete.
Then, the subject's Eustachian tube function will be tested in the ear/ears that have open tympanostomy tubes in the eardrum. For these tests, the subject will be seated comfortably in a chair and a soft rubber tube will be put partway into their ear canal. This tube is attached to a machine that can change the pressure in the ear and measure the pressure at which the Eustachian tube opens and closes, as well as how easily air flows through the Eustachian tube and how easily the subject can open their Eustachian tube during swallowing. These tests only require that the subject not pull the ear plug from their ear and perform certain procedures designed to open their Eustachian tube such as swallowing with an open and pinched nose, blowing against a closed nose and deep breathing. The total time for testing is about 20 minutes per ear.
Then, a study doctor will apply topical medicines by spray and cotton balls to the inside of the nose to decrease any swelling and numb the nose (4% Lidocaine and 0.05% Oxymetazoline mixed in 1:1 proportion). After a short break of about 20 minutes to allow time for these medicines to work, the study doctor will choose which side of the subject's nose is most open and will introduce a small video telescope (called an endoscope) into that side of the nose and move it to the back of the nose. This will allow him/her to see the back of the nose and the Eustachian tubes. He/she will focus the endoscope on the Eustachian tubes and will record video images of the back of the nose, the Eustachian tubes at rest and the movements of the Eustachian tubes while the subject swallows, yawns, repeats an "O" sound, repeats a "K" sound and moves their jaw. The subject will be able to see the movements of the Eustachian tube on a monitor while performing these procedures. This procedure should take about 40 minutes to complete.
After this test, the study is complete.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Keywords
Explore important study keywords that can help with search, categorization, and topic discovery.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
chronic otitis media
adults who have had tympanostomy tube(s) inserted for chronic otitis media
No interventions assigned to this group
Eustachian tube dysfunction
adults who have had tympanostomy tube(s) inserted for the clinical diagnosis of Eustachian tube dysfunction
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* at least one functioning tympanostomy tube
Exclusion Criteria
* otitis onset attributable to barotrauma (eg, hyperbaric oxygen treatment)
* known vestibular/inner ear pathology who may incur dizzy or vertigo symptoms as a result of increase in middle ear pressure
* history of ossicular chain reconstruction
* known hypersensitivity to topical medicines (lidocaine, oxymetazoline)
* severe nasal obstruction
18 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
National Institute on Deafness and Other Communication Disorders (NIDCD)
NIH
University of Pittsburgh
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Cuneyt M. Alper
Professor of Otolaryngology
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Cuneyt M Alper, MD
Role: PRINCIPAL_INVESTIGATOR
Department of Otolaryngology, University of Pittsburgh School of Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Middle Ear Physiology Laboratory, Children's Hospital of Pittsburgh of UPMC
Pittsburgh, Pennsylvania, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PRO09040437
Identifier Type: -
Identifier Source: org_study_id