Gas Supply, Demand and Middle Ear Gas Balance -- Diagnosis of Eustachian Tube Dysfunction

NCT01974726 | Terminated

• 2 other identifiers: PRO13040671-32P50DC007667
• Study Type: interventional
• Target: 95
• Locations: 1 country
• Sites: 1

Brief Summary

The aim of this study is to determine which of the many Eustachian tube function tests (or combination of tests) is most helpful in finding out what is causing ear problems in children and adult patients with middle-ear diseases thought to be due to poor Eustachian tube function. The Eustachian tube is a biological tube that connects the middle ear to the back of the nose and throat. When the Eustachian tube works normally, it opens and closes to help keep the pressure in the middle ear the same as room air-pressure (atmospheric pressure). When the Eustachian tube does not work well, the pressure in the middle ear can increase or decrease and feel like a blocked ear or cause ear pain. Poor Eustachian tube function can be associated with distressing middle-ear symptoms, predispose to middle-ear problems under conditions of rapidly changing air pressures such as occur during airflight and diving, and cause certain middle-ear diseases such as otitis media with effusion. It is also known that the results for the most commonly used Eustachian tube function tests in adults and children with various middle-ear diseases are poorer when compared to children and adults without middle-ear diseases. However, knowing that there is a difference in test results between groups with and without disease does not mean that any of those tests provide information useful in the management of individual patients with diseases due to Eustachian tube function. To be useful clinically, a test(s) that can accurately identify patients with a level of poor Eustachian tube function sufficient to cause middle-ear symptoms and signs and/or cause middle-ear disease is needed. To be very useful, tests should be able to diagnose the cause of any observed Eustachian tube problem so that treatment for that problem could be begun. The investigators would also want tests that could predict whether or not the ear disease will resolve with (or without) treatment and whether or not certain surgical procedures for middle-ear problems will be successful. Here, a number of Eustachian tube function tests are being used to diagnose and characterize the cause of Eustachian tube dysfunction in children and adults presenting to the research clinic with suspected poor Eustachian tube function and/or a recent history of middle-ear disease that can be caused by poor Eustachian tube function. After the testing, medical records will be periodically reviewed for 2 years and study participants will be contacted by phone to obtain information on their middle-ear disease, the response of the disease to any treatments and the success/failure of any surgical procedures used to fix middle-ear problems. Because this study focuses on evaluating the potential usefulness of Eustachian tube function testing for the diagnosis of Eustachian tube dysfunction and, if present, its cause, no specific treatments or surgical interventions are included in this study or recommended by the investigators. These decisions are left to the subject-patient in consultation with their doctor. To further evaluate the Eustachian function tests, a control group of healthy adults without a history of middle-ear problems will undergo testing at two separate sessions; these subjects will have no further follow-up.

Conditions

Eustachian Tube Dysfunction

Keywords

ear; middle ear; Eustachian tube; Eustachian tube dysfunction; Eustachian tube function

Outcome Measures

Primary Outcomes (1)

• ETF tests

  sensitivity/specificity of various ETF tests and combinations of tests

  2 years (affecteds), 1 week (controls)

Study Arms (4)

affected, intact tympanic membranes

OTHER

History of middle-ear disease, ears with no holes/perforations/patent tympanostomy tubes in eardrum

Other: ET Stress test; Other: Sonotubometry; Other: Maneuver Sequence; Other: 9-Step Test; Other: Tubomanometry; Other: Videoendoscopic assessment of ETF

affected, non-intact tympanic membranes

OTHER

History of middle-ear disease, ears with hole/perforation/patent tympanostomy tube in eardrum

Other: ET Stress test; Other: Sonotubometry; Other: Forced Response Test (FRT); Other: Inflation Deflation Test (IDT); Other: Maneuver Sequence; Other: Tubomanometry; Other: Videoendoscopic assessment of ETF

controls, intact tympanic membranes

OTHER

No history of middle-ear disease, ears with no hole/perforation/patent tympanostomy tube in eardrum

Other: Sonotubometry; Other: Maneuver Sequence; Other: 9-Step Test; Other: Tubomanometry; Other: Videoendoscopic assessment of ETF; Other: Pressure chamber ET test

controls, non-intact tympanic membranes

OTHER

No history of middle-ear disease, ears with hole/perforation/patent tympanostomy tube in eardrum

Other: Sonotubometry; Other: Forced Response Test (FRT); Other: Inflation Deflation Test (IDT); Other: Maneuver Sequence; Other: Tubomanometry; Other: Videoendoscopic assessment of ETF

Interventions

ET Stress test OTHER

Performed in pressure chamber. For subjects with intact tympanic membranes, chamber pressure increased from ambient to +2500 daPa (+2000 daPa for children). At that pressure and then at down-stepped pressures of 250 daPa/steps to a chamber pressure of -1500 daPa (or a passive ET opening), the subject will swallow to attempt to open the ET as detected by sonotubometry and/or a change in ear canal pressure. ET passive opening and closing pressures will then be determined. In ears with a non-intact tympanic membrane, a small volume probe connected to a pressure transducer will be placed in the ear canals and the procedure repeated with continuous recording of ME pressure. ET opening is recorded as a change in ME pressure toward local ambient.

affected, intact tympanic membranes; affected, non-intact tympanic membranes

Sonotubometry OTHER

Microphones are placed in the ear canals and covered with ear protectors. A nasal probe placed in one nostril introduces a white noise to the nasopharynx and the subject is asked to swallow. The test system identifies the sound frequency best transmitted through an open ET (if the test is positive, i.e. ET opens) and the procedure is repeated with the nasal sound pressure delivered at that frequency. The probe is then placed in the contralateral nostril and the procedure repeated. The microphone signals from both ear canals are continuously outputted and recorded. A positive ET opening is defined as a 5 dB increase above baseline during any of the 4 swallows and can be semi-quantified as the area under the baseline-adjusted ear canal sound pressure-time curve. The test is designed to measure the presence or absence of muscle-assisted ET openings during swallowing at local ambient pressure.

affected, intact tympanic membranes; affected, non-intact tympanic membranes; controls, intact tympanic membranes; controls, non-intact tympanic membranes

Forced Response Test (FRT) OTHER

The FRT requires a non-intact tympanic membrane and uses an instrument consisting of an ear canal probe coupled serially to a differential pressure transducer, via a valve to a flow sensor and via a second valve to a variable-speed constant-flow pump. The probe is sealed in the ear canal and both valves are opened. The pump is set to deliver a constant flow of 11 ml/min which increases ME pressure to passively open the ET. This is followed by a decrease in ME pressure to steady state pressure and flow conditions. The subject is asked to swallow which either transiently increases (further ET dilation) or decreases (ET constriction) the transET flow. The pump is turned off causing the ET to close at a residual ME pressure. This procedure is repeated at flow rates of 23 and then 46 ml/min.

affected, non-intact tympanic membranes; controls, non-intact tympanic membranes

Inflation Deflation Test (IDT) OTHER

The IDT requires a non-intact tympanic membrane and uses the FRT instrument. ME pressure is increased to 250 daPa (ref ambient), the valves to the flow sensor and pump closed and the subject is asked to swallow repeatedly at a natural interval while monitoring ME pressure until further swallowing fails to change ME pressure. The procedure is repeated with an applied under-pressure of -250 daPa. The outcome variable is the percent pressure change (%reduction) at test end. The test measures the muscle-assisted tubal openings under minor stress (ME under-pressure) and facilitative (ME over-pressure) conditions, and can detect a patulous/semi-patulous ET by an inability to maintain applied ME over and/or under-pressures between swallows.

affected, non-intact tympanic membranes; controls, non-intact tympanic membranes

Maneuver Sequence OTHER

The sequence consists of the Toynbee, Valsalva, Sniffing and Continuous Pressure Test (CPT). The test system consists of ear canal and nasal pressure probes. For the Toynbee test the subject pinches both nostrils (without constricting the nasal probe) and swallows; for the Sniffing test, the subject performs a series of forcible sniffs that must achieve a nasopharyngeal pressure of at least -400 daPa; for the Valsalva test the subject pinches both nostrils and forcibly blows against the closed nose to achieve a nasopharyngeal pressure of at least 400 daPa, and for the CPT the subject breathes through his/her mouth in a relaxed manner for 2 minutes.

affected, intact tympanic membranes; affected, non-intact tympanic membranes; controls, intact tympanic membranes; controls, non-intact tympanic membranes

9-Step Test OTHER

This test requires an intact tympanic membrane. Middle ear (ME) pressure is recorded by tympanometry before and after application of a 300 daPa over-pressure to the ear canal and then before and after application of a 300 daPa under-pressure to the ear canal. Between steps, the subject is asked to swallow in an attempt to open the ET and change ME pressure. A positive test is indicated by a minimum 10 daPa change in ME pressure after a given swallow and excellent muscle-assisted ET opening is indicated by an initial change to a more negative ME pressure after a swallow, followed by a return to 0 daPa, a positive ME pressure and a return to 0 daPa for sequential swallows. The test is designed to measure the presence/absence of active ET openings during swallowing at ambient pressures.

affected, intact tympanic membranes; controls, intact tympanic membranes

Tubomanometry OTHER

The test system is commercially available and can test ears with and without an intact tympanic membrane. Pressure sensors are inserted bilaterally into the ear canals and sealed. A controlled air-flow is introduced into the nose and nasopharynx and the subject swallows. ET openings are detected as a change in ME pressure measured directly as a pressure pulse in the ear canal for ears with a non-intact tympanic membrane or indirectly as a change in ear canal pressure caused by tympanic membrane displacement in ears with intact tympanic membranes. The outcome is the detection of a pressure change in the ear canal during swallowing which is indicative of a muscle-assisted tubal opening.

affected, intact tympanic membranes; affected, non-intact tympanic membranes; controls, intact tympanic membranes; controls, non-intact tympanic membranes

Videoendoscopic assessment of ETF OTHER

The subject's nose is topically anesthetized and decongested with 4% lidocaine and 0.05% oxymetazoline. If ventilation tubes are present, probes are sealed in the ear canal(s)and a pressure of 200 daPa is applied to the ME(s) to assess ET opening. If tympanic membranes are intact, microphones for sonotubometry are placed in the ear canals. Then, an endoscope attached to a video camera is introduced into the ipsilateral nasal cavity and focused on the ET orifice. For sonotubometry, the sound source probe is placed in the contralateral nostril. The subject is asked to swallow, vocalize and perform a series of mandibular movements. Signals from the video camera and pressure transducer or sonotubometry microphones are continuously recorded. The data are studied to document dilation of the nasopharyngeal ET orifice during swallowing and to rule in or out an anatomical or functional nasopharyngeal abnormality as the cause of a diagnosed ET dysfunction.

affected, intact tympanic membranes; affected, non-intact tympanic membranes; controls, intact tympanic membranes; controls, non-intact tympanic membranes

Pressure chamber ET test OTHER

Performed in pressure chamber. Pressure increased to create middle-ear underpressure, then subject is asked to swallow several times. Middle-ear pressures are then measured by tympanometry. This is repeated with decreased chamber pressure, creating a middle-ear overpressure.

controls, intact tympanic membranes

Eligibility Criteria

• Age: 3 Years - 70 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• years of age
• Diagnosed or suspected Eustachian tube dysfunction or middle-ear disease
• Able to read and comprehend English

You may not qualify if:

• Extant middle-ear effusion, allergic rhinitis or "cold" (may enter when resolved)
• History of ossicular reconstruction
• Blood pressure greater than or equal to 140/90 (adults)
• Recent angina; history of heart attack, stroke, cardiac surgery or any other medical condition that the study physician deems entry not in the subject's best interest.
• CONTROL SUBJECTS
• years of age
• Generally healthy
• No history of middle-ear disease
• Intact or non-intact tympanic membrane -- perforation or tube for reasons other than middle-ear disease.
• Extant middle-ear effusion, allergic rhinitis or "cold" (may enter when resolved)
• History of ossicular reconstruction
• Blood pressure greater than or equal to 140/90
• Sensitivity to drugs used for endoscopy (lidocaine, oxymetazoline)

Sponsors & Collaborators

• University of Pittsburgh: lead
• National Institute on Deafness and Other Communication Disorders (NIDCD): collaborator

Study Sites (1)

University of Pittsburgh Middle Ear Physiology Laboratory

Pittsburgh, Pennsylvania, 15213, United States

Location

Study Officials

• Cuneyt M Alper, MD

  University of Pittsburgh

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor of Otolaryngology

Study Record Dates

• First Submitted: October 22, 2013
• First Posted: November 1, 2013
• Study Start: October 1, 2013
• Primary Completion: June 27, 2019
• Study Completion: June 27, 2019
• Last Updated: October 8, 2020

Record last verified: 2020-10

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)