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The Accuracy of Sonotubometry to Assess the Eustachian Tube

Assessing the Sensitivity and Specificity of Sonotubometry to Measure the Eustachian Tube Function

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05740384
Enrollment
28
Registered
2023-02-23
Start date
2023-04-21
Completion date
2023-12-30
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eustachian Tube Dysfunction

Keywords

obstructive Eustachian tube dysfunction, Eustachian tube dysfunction

Brief summary

The Eustachian tube (ET) connects the middle ear with the throat and is important for maintaining a healthy middle ear. Sonotubometry is a new method to measure how well the ET works by using sound. A speaker is placed at the nostril and a microphone records sound in the external ear canal. The ET is closed at rest and opens with swallowing. This is measured as an increase in sound measured in the external ear by sonotubometry. Previous research has not proven that sonotubometry is reliable enough to be used in clinics to assess ET dysfunction (a disease where the ET does not open properly). In a recent study with healthy volunteers, it was possible to identify many of the existing issues of sonotubometry and improve the reliability of this method. This was primarily achieved by testing different sound types and sound volumes. This study aims to assess the reliability and usability of the new testing protocol in study participants with ET dysfunction. The results of this study will then be compared with the results from the previous study with healthy volunteers to work out how well sonotubometry works. Ultimately, this research aims to improve the ability to diagnose ET dysfunction.

Interventions

DEVICESonotubometry Assessment

The exact order of the measurements will be randomised: * Recording type 1: No sound applied, 10 seconds recording of baseline noise, followed by recording when the participant is asked to swallow 3 times. * Recording type 2: White noise applied, 10 seconds recording of baseline noise, followed by recording when the participant is asked to swallow 3 times. * Ask for subjective feedback (did you hear a change in the sound in your ear on swallowing?) after each recording * This is repeated using the contralateral ear and nostril. After successful recording, the microphone will be removed. For comparison, tubomanometry measurements will be performed on each ear. Tubomanometry is an alternative method to assess the middle ear and Eustachian tube. Afterwards, the participant's involvement in the study will be complete. The entire involvement will take about 50 minutes.

Sponsors

University of Cambridge
CollaboratorOTHER
James Tysome
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

The order of the assessment measurements is batch-wise randomised but there is no masking. Both the participant and investigator know what sort of measurements is being performed.

Intervention model description

This is a validation study in 28 ears with Eustachian tube dysfunction.

Eligibility

Sex/Gender
ALL
Age
16 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Participant is capable of giving informed consent (in the English language) * Participant has a current diagnosis of obstructive Eustachian tube dysfunction in the ear clinic at Addenbrooke's Hospital * Age 16 and over

Exclusion criteria

* Cardiac pacemaker (incompatible with the large sonotubometry speaker magnet) * Discharging or infected ear (for infection control reasons) * Otitis Media with effusion (complicates test interpretation) * Cleft palate or Craniofacial abnormalities (complicates test interpretation) * Cholesteatoma (complicates test interpretation) * Nasopharyngeal mass (complicates test interpretation) * History of radiotherapy to the head and neck (can affect surrounding tissue structure)

Design outcomes

Primary

MeasureTime frameDescription
Assess Specificity and Sensitivity of Sonotubometry using a Custom-Built Sonotubometer40-50 minutesThe main objective of the trial is to measure the specificity and sensitivity of an assessment method of the Eustachian tube called sonotubometry. To do this, eight sonotubometry measurements will be performed on each patient using the custom built Sonotubometry device. In total a maximum of 28 patients will be measured. This data will be compared to measurements from volunteers (data collected through a different study) to measure the sensitivity and specificity in percentage.

Secondary

MeasureTime frameDescription
Ability of Sonotubometry Measurements to detect Eustachian tube opening by using an Increased Sound Amplitude40-50 minutesThe secondary objective is to assess if sonotubometry with an sound amplitude of 120dB is able to detect Eustachian tube opening. In the past a lower sound level was used (below 110dB) and thus the goal here is to measure the suitability of a higher sound pressure for sonotubometry. This will be measured by the ability of the new method to reliably detect the Eustachian tube function in patients and healthy volunteers (healthy volunteers data was gathered in a separate study)

Countries

United Kingdom

Contacts

Primary ContactTobia Nava, MSc
tsn23@cam.ac.uk0044 7311213580
Backup ContactJames Tysome, Dr
jrt20@cam.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026