Could Ultra-Low-Dose CT reshape emergency pneumonia imaging workload?
NCT ID NCT07870525
First seen Oct 13, 2026 · Last updated Oct 14, 2026 · Updated 1 time
Summary
Researchers at the University of Southern Denmark compare how much staff time two chest imaging methods require when adults arrive at the emergency department with suspected community-acquired pneumonia. One method is conventional chest radiography, the other is ultra-low-dose chest computed tomography. The study measures cumulative staff person-minutes per imaging episode, from when staff fetch the patient to when a final radiological report is ready. About 66 adults who can undergo the assigned scan take part during weekday daytime hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ultra-low-dose chest computed tomography (ULDCT) compared with conventional chest radiography
- What this could lead to
- If ultra-low-dose CT uses staff time efficiently, hospitals could weigh it against chest X-rays when planning emergency imaging for suspected pneumonia.
- What could go wrong
- This small study measures staff time, not whether patients get better or are diagnosed more accurately. Its results may not apply to hospitals with different staffing or equipment.
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 66 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2025
- Expected to finish
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Jun 2027
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
Patients from Emergency Department from Hospital Sonderjylland, Aabenraa, Denmark.
- 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: * Patients presenting to the emergency department during daytime weekday hours in whom CAP is a differential diagnosis, and who are able to undergo the assigned imaging examination. Exclusion Criteria: * Patients requiring immediate imaging for a critical condition (for example suspected pneumothorax). * Bariatric patients exceeding the technical limits of the scanner * Pregnancy * Patients requiring additional imaging beyond the chest (for example abdominal CT) * Severe dementia, or need for sedation to complete imaging * Patients requiring mechanical ventilation. * Patients requiring accompaniment by medical staff during transport
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Sønderjylland
RECRUITINGAabenraa, 6200, Denmark
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