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RecruitingNCT05686941Updated Feb 22, 2024

Is Laryngeal Ultrasound Useful in the Assessment for ILO? A Protocol for a Two-stage Exploratory Pilot Study

An observational study in Vocal Cord Dysfunction, Asthma Brittle and Inducible Laryngeal Obstruction, sponsored by Lancashire Teaching Hospitals NHS Foundation Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-02-22.

Sponsored by Lancashire Teaching Hospitals NHS Foundation Trust · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years and older
Sex
All
01

Study summary

This study is a feasibility study to see if an ultrasound scan of the vocal cords can detect narrowing of the vocal cords as seen in a condition called inducible laryngeal Obstruction (the vocal cords narrow or close on breathing in, which makes it very difficult to breathe).

Read the detailed description

This study aims to help understand whether viewing the vocal cords with an ultrasound device is useful to detect the movement of the vocal cords during breathing. This study is useful, as some people who have abnormal movements of the vocal cords on breathing in find it more difficult to breathe in, and often this leads to a big impact on their quality of life. It may also mean they are on medications that they may not need not be on, as abnormal movements of the vocal cords can often be mistaken for asthma, so they may have been placed on asthma medication when they may not need to be.

Usually, the way the abnormal movements of the vocal cords are seen now is via a small camera is placed via the nose into the throat to directly look at the vocal cords. Some people find this uncomfortable and may have to wait for a long time for it to happen. Also, this procedure is expensive, and is done in an endoscopy theatre, which may make it more daunting for some people, and make the wait longer. There are only a few centres that do these assessments with the camera, so people may have to travel some distance to have an assessment.

It is hoped, by doing this study, the investigators can see whether ultrasound can help assess if people have abnormal vocal cord movements when they breathe in. This will be done in 2 stages, one with healthy volunteers, and the second stage in patients who have been referred for assessment of their vocal cords to see if they have abnormal movements when breathing in. The investigators will also ask the volunteers and patients what their experience of having the ultrasound was like, and will ask the patients in the study how the ultrasound scan felt, when compared to the camera test

02

Conditions studied

  • Vocal Cord Dysfunction
  • Asthma Brittle
  • Inducible Laryngeal Obstruction
  • Paradoxical Vocal Fold Motion

Keywords

  • Inducible laryngeal obstruction
  • Ultrasound
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

  • No definite signs or symptoms of vocal fold paralysis
  • No of history laryngeal surgeries
  • No history of pathology pathology
  • Too anxious to undergo procedure

Inclusion criteria

Healthy volunteers:

  • No definite signs or symptoms of vocal fold paralysis
  • No voice change
  • No history laryngeal surgeries
  • No History of pathology
  • No uncontrolled Respiratory disease

Exclusion criteria

Exclusion Criteria:

  • Participants with a known vocal fold pathology
  • Participants with a history of head and neck surgery.
04

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • Healthy Volunteers

    Employees of the Host organisation in the Respiratory Team who meet the inclusion criteria

    Other: Trans-cutaneous Laryngeal ultrasound (TLUS)

  • Patients with suspected Inducible laryngeal Obstruction (ILO)

    Patients referred to a Tertiary referral centre who are suspected of having ILO

    Other: Trans-cutaneous Laryngeal ultrasound (TLUS) · Other: TLUS and simultaneous laryngoscopy

Interventions

  • OtherTrans-cutaneous Laryngeal ultrasound (TLUS)

    Assessment of the larynx (specifically the vocal cords) with hand held portable ultrasound device to assess the movements of the vocal cords

  • OtherTLUS and simultaneous laryngoscopy

    Assessment of the larynx (specifically the vocal cords) with hand held portable ultrasound device to assess the movements of the vocal cords with simultaneous video laryngoscopy (usual care)

    Also known as: TLUS

05

What researchers measure

Primary outcomes

  1. Number of vocal cords that are seen with the ultrasound

    Can the vocal cord be seen under TLUS for Healthy Volunteers? Numeric data.

    Time frame: 1 day

  2. Number of particpants where visualisation of mimicked inspiratory adduction is visible on ultrasound

    Can the vocal cords be seen to adduct under TLUS when healthy volunteers mimic ILO? Binary outcome: yes or no.

    Time frame: 1 day

  3. To assess the sensitivity, specificity and positive predictive value of the use of ultrasound

    To assess the sensitivity, specificity and positive predictive value of the use of ultrasound in the assessment of ILO, using Laryngoscopy as reference standard in the patient population (n=30)

    Time frame: 1 day

  4. Questionnaire Investigating user perspectives on the acceptability of TLUS

    A qualitative questionnaire investigating the patient and healthy volunteer perspectives on their experiences of undergoing TLUS assessment of the vocal cords. The questionnaire will look at the acceptability of the assessment in terms of comfort, repeatability, and comparison with laryngoscopy (for patients only).

    Time frame: 1 day

06

Study locations

1 of 1 sites recruiting
  • Lancashire Teaching Hospitals NHS Trust
    Preston, Lancashire PR2 9HT, United Kingdom
    Recruiting
07

References and documents

Study documents

  • Protocol and statistical analysis plan · Jul 18, 2022
  • Informed consent form · Jul 18, 2022

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

08

Registry details

Key details

Study ID
NCT05686941
Lead sponsor
Lancashire Teaching Hospitals NHS Foundation Trust
Collaborators
Edge Hill University, University College, London, Lancaster University, University of Central Lancashire
Responsible party
Claire Slinger (Consultant Speech & Language Therapist, Lancashire Teaching Hospitals NHS Foundation Trust) — Principal investigator
First posted
Jan 17, 2023
Start date
Aug 24, 2022
Primary completion
Jun 27, 2025 (estimated)
Completion
Jun 27, 2025 (estimated)
Last update
Feb 22, 2024

Study contacts

Claire Slinger
Contact
claire.slinger@lthtr.nhs.uk
01171523237
Kina Bennett
Contact
kina.bennett@lthtr.nhs.uk
Kina Bennett
study chair · Lancashire Teaching Hospitals NHS Trust
Claire Slinger
principal investigator · Lancashire Teaching Hospitals NHS Trust

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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