Can a simple test combo pinpoint asthma faster?
NCT ID NCT07792213
First seen Aug 28, 2026 · Last updated Aug 28, 2026
Summary
This study compares common diagnostic tests for asthma in adults to see which ones, alone or combined, most accurately identify the condition. Participants with suspected asthma will undergo spirometry, FeNO, oscillometry, and a bronchial provocation challenge. Researchers will compare test results against the final diagnosis to measure accuracy, and also examine how obesity and normal spirometry affect results. The goal is to improve diagnostic accuracy and speed up care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Diagnostic tests: spirometry, fractional exhaled nitric oxide (FeNO), oscillometry, and bronchial provocation testing
- What this could lead to
- If successful, this could lead to faster and more accurate asthma diagnoses, reducing unnecessary tests and improving care for people with suspected asthma.
- What could go wrong
- This is a diagnostic accuracy study, not a treatment trial. Results may not apply to all populations, and the tests may not perform as well in real-world settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 2,176 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Jul 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Potential participants will be identified from adults referred to the Physiological Sciences Department at George Eliot Hospital NHS Trust for objective investigation of suspected asthma through routine primary or secondary care referral pathways. Eligible participants will be assessed by the research team. Only patients who provide written informed consent will be enrolled into the study. Following consent, the lead researcher will access relevant electronic healthcare records to collect the clinical information required for the study, as described in the consent form. Study data will be assigned a unique pseudonymised study identification number and stored securely, password-protected, on the Trust's systems. Access to identifiable information will be restricted to authorised members of the research team in accordance with the UK GDPR, the Data Protection Act 2018 and NHS information governance policies.
- Ages
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16 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * •Adults aged 16years and older * Referral for objective investigation of suspected asthma * Ability to provide written informed consent Exclusion Criteria: * Previous confirmed diagnosis of asthma or other chronic airways disease * Respiratory tract infection within six weeks prior to testing * Current smoker or ex-smoker with a greater than 10p\\pack-year smoking history * Inability to perform pulmonary function testing to acceptable technical standards * Contraindications to any of the diagnostic investigations as per departmental guidelines * Lack of capacity to provide informed consent
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Physiological Sciences
Nuneaton, North Warwickshire, CV10 7DJ, United Kingdom
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