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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05686941
Other study ID # 298631
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date August 24, 2022
Est. completion date June 27, 2025

Study information

Verified date February 2024
Source Lancashire Teaching Hospitals NHS Foundation Trust
Contact Claire Slinger
Phone 01171523237
Email claire.slinger@lthtr.nhs.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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).


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


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 27, 2025
Est. primary completion date June 27, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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: - Participants with a known vocal fold pathology - Participants with a history of head and neck surgery.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Trans-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
TLUS 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)

Locations

Country Name City State
United Kingdom Lancashire Teaching Hospitals NHS Trust Preston Lancashire

Sponsors (5)

Lead Sponsor Collaborator
Lancashire Teaching Hospitals NHS Foundation Trust Edge Hill University, Lancaster University, University College, London, University of Central Lancashire

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of vocal cords that are seen with the ultrasound Can the vocal cord be seen under TLUS for Healthy Volunteers? Numeric data. 1 day
Primary 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. 1 day
Primary 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) 1 day
Primary 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). 1 day
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