ER study: CT scans sharpen pneumonia diagnosis
NCT ID NCT01574066
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 339 emergency room patients with suspected pneumonia to see if a chest CT scan could improve diagnosis. The goal was to find out if the CT scan changed the doctor's initial diagnosis, and if it led to changes in antibiotic treatment or hospital admission decisions. The results help understand the value of CT scans for diagnosing pneumonia in urgent care 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.
- Phase
-
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
-
339 people
The number who actually took part.
- Start date
-
Nov 2011
- Finished
-
Jul 2013
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Patient above 18 years of age * Patient with a presumptive diagnosis of CAP according to attending ED physician * Patient experiencing at least one systemic sign (T°\>38°C or \< 36°C, HR\>90/min, RR\>20/min) * Patient experiencing one respiratory sign (cough, lateral chest pain, localized crackles, dyspnea) that recently appeared * Patient with a prior medical examination, the results have been or will be communicated * Patient gave written informed consent or in cases of emergency parent/ support person who gave written informed consent if he/she is present on the day of inclusion Exclusion Criteria: * Pregnancy * Patient with shock * Patient with respiratory distress and immune suppression * Patient with other criteria for immediate ICU referral to ICU * Patient with living conditions making it impossible to follow 28 days * Patient not affiliated with a social security system
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Community-acquired pneumonia are added.
Genom att skicka in godkänner du våra Användarvillkor
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
-
Bichat Hospital
Paris, 75018, France
-
Cochin Hospital
Paris, 75014, France
-
La Pitié Salpêtrière Hospital
Paris, 75013, France
-
Tenon Hospital
Paris, 75020, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Three oxygen sensors, one question: can site differences flag the sickest breathless patients?
- Blood test vs. clinical check: which safely cuts antibiotic use in pneumonia?
- Can a handheld breathing device and phone app help COPD patients breathe easier?
- Can a video call save a Child's life? emergency triage goes visual
- A simple breath: could guided breathing calm heart failure symptoms?
- Can a touch on the hands ease Asthma's breathlessness and sleeplessness?