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Relationship Between Acoustic Breath Sounds and Spirometry

U

University Hospitals Birmingham NHS Foundation Trust (UHB)

Status

Enrolling

Conditions

Asthma COPD

Treatments

Device: Wheeze measurement

Study type

Interventional

Funder types

Other

Identifiers

NCT06039943
RKK7649

Details and patient eligibility

About

The goal of this clinical trial is to assess whether wheeze as assessed by a commercially available wheeze monitor is comparable to lung function as measured during a spirometry test. The main questions it aims to answer are whether measures of airflow obstruction (FEV1, FEV1/FVC, PEF) correlate with wheeze score (Tw/Ttot%).

Participants consenting to take part will undergo wheeze measurement prior to and during a spirometry test and will be asked to complete a series of symptom questionnaires.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Consenting adult (aged 18-95) University Hospitals Birmingham patient's attending the Lung Function and Sleep Department (LF&S) routinely as part of their standard clinical management pathway for Lung Function testing that includes Spirometry assessments.
  • All patients irrespective of condition will be approached to participate.

Exclusion criteria

  • Subjects who are contraindicated to perform spirometry on the day of testing
  • Subjects who cannot speak or read English
  • Patients accessing non-adult services
  • Subjects who are unable or do not wish to consent
  • Patients with known or suspected restrictive lung disease

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

200 participants in 1 patient group

All participants
Experimental group
Description:
Participants will undergo wheeze monitoring during tidal breathing prior to spirometry and during a spirometry test.
Treatment:
Device: Wheeze measurement

Trial contacts and locations

1

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Central trial contact

Richard Glover; Brendan Cooper, PhD

Data sourced from clinicaltrials.gov

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