New tests aim to cut unnecessary antibiotics for lung infections in hospitals
NCT ID NCT05483309
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at whether using CT scans and a rapid sputum test (FilmArray) can improve diagnosis of hospital-acquired pneumonia (HAP). Currently, chest X-rays are often unclear, leading to misdiagnosis and overuse of antibiotics. The trial enrolled 220 adults with suspected HAP to see if these modern tests could help doctors give the right antibiotics faster. Since this is a feasibility study, its main goal was to see if a larger, more definitive trial is possible.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CT scan and FilmArray Pneumonia Panel (rapid sputum test)
- What this could lead to
- If successful, this could lead to a larger trial that shows how to diagnose hospital-acquired pneumonia more accurately, reduce unnecessary antibiotics, and slow antibiotic resistance.
- What could go wrong
- This is a small feasibility study, not a full trial. It only checks if a larger trial is possible, so it won't directly prove that these tests improve patient outcomes.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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220 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Jun 2025
- 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.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: Stage 1: * Age ≥ 18 years * Suspected HAP\* For the purposes of this study, HAP is defined as per the BTS and FDA definitions i.e. pneumonia which develops 48 hours after an admission to hospital for an alternative diagnosis; or a new presentation to hospital with pneumonia in a patient who has been discharged from an overnight stay in hospital within the last 10 days. Stage 2: * The clinician intends to treat the patient for HAP or a hospital acquired respiratory tract infection (RTI). * A sputum sample has been obtained before 2nd dose of antibiotic. Exclusion Criteria: Stage 1: * Already received a chest X-ray to confirm suspected HAP diagnosis * Diagnosis or suspected diagnosis of ventilator acquired pneumonia * Intention to palliate rather than cure * Interventions cannot be completed before administration of second antibiotic dose\* * Cannot be randomised to low-dose, non-contrast CT scan on clinical grounds e.g. strong suspicion of PE\*\* * Pregnancy\*\*\* * Previous study participation (patients with second of third episodes of HAP will not be re-recruited) In the circumstance where a patient is diagnosed with HAP whist receiving antibiotics for a non-respiratory infection e.g. cellulitis or UTI, if the HAP diagnosis leads to a change in the antibiotic prescription to cover the HAP then that patient will be eligible for recruitment. However, if the diagnosis of HAP does not result in a change in antibiotic then the patient is not eligible. A non-contrast, low-dose thoracic CT scan is an inappropriate test for a PE and if that is high in the differential diagnosis then tick yes here. A urine pregnancy test is required as part of routine care prior to a chest X-ray or CT scan. If the test reveals the patient is pregnant, they will not be eligible for the study as they will be unable to receive a CT scan as part of this study. Pregnancy tests are not required at future time points. Stage 2: \- Following the CXR or CT the clinician decides not to treat with antibiotics for either HAP or a hospital acquired RTI.
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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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Lancashire teaching hospitals NHS Foundation Trust
Preston, United Kingdom
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Liverpool University Hospitals NHS Foundation Trust
Liverpool, L69 7BE, United Kingdom
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Manchester University NHS Foundation Trust
Manchester, United Kingdom
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